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  <description><![CDATA[<p>Discussing issues that impact scientific research monthly, from clinical research to ethical considerations. Hosted by Alexa McClellan. New episode every month. Learn more at about.citiprogram.org</p>]]></description>
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    <itunes:title>The Belmont Report at Belmont: Voices of Research Ethics - On Research Podcast</itunes:title>
    <title>The Belmont Report at Belmont: Voices of Research Ethics - On Research Podcast</title>
    <itunes:summary><![CDATA[In this special episode of On Research, host Alexa McClellan travels to Belmont Manor and Historic Park in Howard County, Maryland—the site where the Belmont Report was drafted nearly 50 years ago. Through conversations with regulators, research professionals, IRB leaders, research participants, and descendants of those impacted by the Tuskegee Syphilis Study, this episode explores the lasting influence of the Belmont Report's principles of Respect for Persons, Beneficence, and Justice. Join ...]]></itunes:summary>
    <description><![CDATA[<p>In this special episode of <em>On Research</em>, host Alexa McClellan travels to Belmont Manor and Historic Park in Howard County, Maryland—the site where the Belmont Report was drafted nearly 50 years ago. Through conversations with regulators, research professionals, IRB leaders, research participants, and descendants of those impacted by the Tuskegee Syphilis Study, this episode explores the lasting influence of the Belmont Report&apos;s principles of Respect for Persons, Beneficence, and Justice. Join us as we reflect on the history that shaped modern human research protections, examine the role of trust and trustworthiness in research today, and consider why the Belmont Report remains as relevant as ever. </p><p> </p><p><b>Notes:</b> </p><ul><li><em>On Tech Ethics –</em> A CITI Program Podcast - <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li><em>Bioethics </em>– A CITI Program Course - <a href='https://about.citiprogram.org/course/bioethics/'>https://about.citiprogram.org/course/bioethics/</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></description>
    <content:encoded><![CDATA[<p>In this special episode of <em>On Research</em>, host Alexa McClellan travels to Belmont Manor and Historic Park in Howard County, Maryland—the site where the Belmont Report was drafted nearly 50 years ago. Through conversations with regulators, research professionals, IRB leaders, research participants, and descendants of those impacted by the Tuskegee Syphilis Study, this episode explores the lasting influence of the Belmont Report&apos;s principles of Respect for Persons, Beneficence, and Justice. Join us as we reflect on the history that shaped modern human research protections, examine the role of trust and trustworthiness in research today, and consider why the Belmont Report remains as relevant as ever. </p><p> </p><p><b>Notes:</b> </p><ul><li><em>On Tech Ethics –</em> A CITI Program Podcast - <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li><em>Bioethics </em>– A CITI Program Course - <a href='https://about.citiprogram.org/course/bioethics/'>https://about.citiprogram.org/course/bioethics/</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></content:encoded>
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    <itunes:title>Beyond Persistence: How Early-Career Scientists Can Thrive - On Research Podcast</itunes:title>
    <title>Beyond Persistence: How Early-Career Scientists Can Thrive - On Research Podcast</title>
    <itunes:summary><![CDATA[In this episode of On Research, host Alexa McClellan speaks with Jim Gould, Director of Postdoctoral Affairs at Harvard Medical School and co-host of Propelling Careers, about what it takes for early-career scientists to thrive in today’s research environment. Together, they explore funding uncertainty, burnout, career flexibility, resilience, mentorship, and the skills researchers need to build sustainable and fulfilling careers. Whether you're a trainee, postdoc, or research professional, t...]]></itunes:summary>
    <description><![CDATA[<p>In this episode of <em>On Research</em>, host Alexa McClellan speaks with Jim Gould, Director of Postdoctoral Affairs at Harvard Medical School and co-host of <em>Propelling Careers</em>, about what it takes for early-career scientists to thrive in today’s research environment. Together, they explore funding uncertainty, burnout, career flexibility, resilience, mentorship, and the skills researchers need to build sustainable and fulfilling careers. Whether you&apos;re a trainee, postdoc, or research professional, this conversation offers practical insights for navigating change while maintaining purpose and research integrity. </p><p><b>Notes:</b> </p><ul><li><em>Propelling Careers </em>Podcast – <a href='https://open.spotify.com/show/6zaZCQ7lScgHepGl0D7LFq'>https://open.spotify.com/show/6zaZCQ7lScgHepGl0D7LFq</a> </li><li><em>Protocol Development &amp; Execution: Beyond a Concept </em>– A CITI Program Course - <a href='https://about.citiprogram.org/course/protocol-development-execution-beyond-a-concept/'>https://about.citiprogram.org/course/protocol-development-execution-beyond-a-concept/</a> </li><li><em>On Campus </em>– A CITI Program Podcast -  <a href='https://www.buzzsprout.com/1896915/'>https://www.buzzsprout.com/1896915/</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></description>
    <content:encoded><![CDATA[<p>In this episode of <em>On Research</em>, host Alexa McClellan speaks with Jim Gould, Director of Postdoctoral Affairs at Harvard Medical School and co-host of <em>Propelling Careers</em>, about what it takes for early-career scientists to thrive in today’s research environment. Together, they explore funding uncertainty, burnout, career flexibility, resilience, mentorship, and the skills researchers need to build sustainable and fulfilling careers. Whether you&apos;re a trainee, postdoc, or research professional, this conversation offers practical insights for navigating change while maintaining purpose and research integrity. </p><p><b>Notes:</b> </p><ul><li><em>Propelling Careers </em>Podcast – <a href='https://open.spotify.com/show/6zaZCQ7lScgHepGl0D7LFq'>https://open.spotify.com/show/6zaZCQ7lScgHepGl0D7LFq</a> </li><li><em>Protocol Development &amp; Execution: Beyond a Concept </em>– A CITI Program Course - <a href='https://about.citiprogram.org/course/protocol-development-execution-beyond-a-concept/'>https://about.citiprogram.org/course/protocol-development-execution-beyond-a-concept/</a> </li><li><em>On Campus </em>– A CITI Program Podcast -  <a href='https://www.buzzsprout.com/1896915/'>https://www.buzzsprout.com/1896915/</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></content:encoded>
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    <itunes:duration>2091</itunes:duration>
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    <itunes:title>Hope, Uncertainty, and the Future of Science - On Research Podcast</itunes:title>
    <title>Hope, Uncertainty, and the Future of Science - On Research Podcast</title>
    <itunes:summary><![CDATA[In a moment of uncertainty across the research landscape, what does it mean to lead with clarity, integrity, and hope? In this episode of On Research, Dr. Josh Fessel shares insights from his experience at the NIH to unpack shifting federal priorities, growing instability, and the real risks of inaction. Together, we explore how researchers and institutions can navigate change, rebuild trust, and stay grounded in science’s core purpose: serving people. Thoughtful, timely, and ultimately hopef...]]></itunes:summary>
    <description><![CDATA[<p>In a moment of uncertainty across the research landscape, what does it mean to lead with clarity, integrity, and hope? In this episode of <em>On Research</em>, Dr. Josh Fessel shares insights from his experience at the NIH to unpack shifting federal priorities, growing instability, and the real risks of inaction. Together, we explore how researchers and institutions can navigate change, rebuild trust, and stay grounded in science’s core purpose: serving people. Thoughtful, timely, and ultimately hopeful—this conversation offers a roadmap for moving forward when the path isn’t clear. </p><p> </p><p><b>Notes:</b> </p><ul><li><em>Conflict Management</em> – A CITI Program Course - <a href='https://about.citiprogram.org/course/conflict-management/'>https://about.citiprogram.org/course/conflict-management/</a> </li><li><em>On Tech Ethics </em>– A CITI Program Podcast -  <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul><p> </p>]]></description>
    <content:encoded><![CDATA[<p>In a moment of uncertainty across the research landscape, what does it mean to lead with clarity, integrity, and hope? In this episode of <em>On Research</em>, Dr. Josh Fessel shares insights from his experience at the NIH to unpack shifting federal priorities, growing instability, and the real risks of inaction. Together, we explore how researchers and institutions can navigate change, rebuild trust, and stay grounded in science’s core purpose: serving people. Thoughtful, timely, and ultimately hopeful—this conversation offers a roadmap for moving forward when the path isn’t clear. </p><p> </p><p><b>Notes:</b> </p><ul><li><em>Conflict Management</em> – A CITI Program Course - <a href='https://about.citiprogram.org/course/conflict-management/'>https://about.citiprogram.org/course/conflict-management/</a> </li><li><em>On Tech Ethics </em>– A CITI Program Podcast -  <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul><p> </p>]]></content:encoded>
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    <pubDate>Wed, 27 May 2026 10:00:00 -0400</pubDate>
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  <psc:chapter start="7:12" title="– Why Dr. Fessel Left NIH" />
  <psc:chapter start="11:55" title="– What Feels Most Different in Science Right Now" />
  <psc:chapter start="16:06" title="– What the Research Community Should Watch in the Next 12 to 24 Months" />
  <psc:chapter start="21:53" title="– Why Quiet Inaction Can Be Dangerous" />
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  <psc:chapter start="38:20" title="– Why There Is Still Reason for Hope" />
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    <itunes:duration>2756</itunes:duration>
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    <itunes:title>Protecting Innovation: COGR’s Guidance on Research Security for Tech Transfer - On Research Podcast</itunes:title>
    <title>Protecting Innovation: COGR’s Guidance on Research Security for Tech Transfer - On Research Podcast</title>
    <itunes:summary><![CDATA[Technology transfer offices are increasingly on the front lines of research security—and the rules are changing fast. In this episode of On Research, we’re joined by Allen DiPalma and Kevin Wozniak from the Council on Governmental Relations (COGR) to unpack COGR’s Research Security Guidance for Technology Transfer and what it means for protecting innovation while still supporting collaboration.   Notes:  Council on Governmental Relations (COGR). 2025. “Research Security Regulations:...]]></itunes:summary>
    <description><![CDATA[<p>Technology transfer offices are increasingly on the front lines of research security—and the rules are changing fast. In this episode of On Research, we’re joined by Allen DiPalma and Kevin Wozniak from the Council on Governmental Relations (COGR) to unpack COGR’s Research Security Guidance for Technology Transfer and what it means for protecting innovation while still supporting collaboration. <br/><br/>Notes: </p><ul><li>Council on Governmental Relations (COGR). 2025. “Research Security Regulations: Practical Considerations for Technology Transfer Professionals.”  - <a href='https://www.cogr.edu/sites/default/files/2025-11/Research%20Security%20Regulations%20Practical%20Considerations.pdf'>https://www.cogr.edu/sites/default/files/2025-11/Research%20Security%20Regulations%20Practical%20Considerations.pdf</a></li><li>Technology Transfer – A CITI Program Course - <a href='https://about.citiprogram.org/course/technology-transfer/ '>https://about.citiprogram.org/course/technology-transfer/ </a></li><li>On Campus – A CITI Program Podcast -  <a href='https://www.buzzsprout.com/1896915/ '>https://www.buzzsprout.com/1896915/ </a></li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog  '>https://about.citiprogram.org/course-catalog  </a></li></ul>]]></description>
    <content:encoded><![CDATA[<p>Technology transfer offices are increasingly on the front lines of research security—and the rules are changing fast. In this episode of On Research, we’re joined by Allen DiPalma and Kevin Wozniak from the Council on Governmental Relations (COGR) to unpack COGR’s Research Security Guidance for Technology Transfer and what it means for protecting innovation while still supporting collaboration. <br/><br/>Notes: </p><ul><li>Council on Governmental Relations (COGR). 2025. “Research Security Regulations: Practical Considerations for Technology Transfer Professionals.”  - <a href='https://www.cogr.edu/sites/default/files/2025-11/Research%20Security%20Regulations%20Practical%20Considerations.pdf'>https://www.cogr.edu/sites/default/files/2025-11/Research%20Security%20Regulations%20Practical%20Considerations.pdf</a></li><li>Technology Transfer – A CITI Program Course - <a href='https://about.citiprogram.org/course/technology-transfer/ '>https://about.citiprogram.org/course/technology-transfer/ </a></li><li>On Campus – A CITI Program Podcast -  <a href='https://www.buzzsprout.com/1896915/ '>https://www.buzzsprout.com/1896915/ </a></li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog  '>https://about.citiprogram.org/course-catalog  </a></li></ul>]]></content:encoded>
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  <psc:chapter start="22:00" title="– Practical Considerations for Sharing Data, Materials, and Technical Agreements" />
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    <itunes:duration>2016</itunes:duration>
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    <itunes:title>Rethinking Child Assent Practices - On Research Podcast</itunes:title>
    <title>Rethinking Child Assent Practices - On Research Podcast</title>
    <itunes:summary><![CDATA[What does meaningful child assent really look like in research? In this episode of On Research, host Alexa McClellan speaks with Dr. David Coker about rethinking child assent beyond procedural compliance. Drawing on his recent scholarship, Dr. Coker explores gaps in current practices, regulatory tensions, inclusion of children with disabilities, and the role of IRBs in supporting assent as a developmentally appropriate, ethical process. The conversation challenges researchers to move from col...]]></itunes:summary>
    <description><![CDATA[<p><b>What does meaningful child assent really look like in research?</b> In this episode of <em>On Research</em>, host Alexa McClellan speaks with Dr. David Coker about rethinking child assent beyond procedural compliance. Drawing on his recent scholarship, Dr. Coker explores gaps in current practices, regulatory tensions, inclusion of children with disabilities, and the role of IRBs in supporting assent as a developmentally appropriate, ethical process. The conversation challenges researchers to move from collecting assent as a formality to practicing it as a genuine expression of respect for children’s autonomy and voice. <br/> </p><p><b>Notes:</b> </p><ul><li>Coker, David C, Ketaki Inamdar, Daniel F. McCleary, and Lesley Cottrell.  2025. “Child Assent Practices in Research: Improving Ethics, Decision-Making, and Inclusivity.” <em>Journal of Educational Research &amp; Practice</em>. 15:1-24. <a href='https://files.eric.ed.gov/fulltext/EJ1492202.pdf'>https://files.eric.ed.gov/fulltext/EJ1492202.pdf</a> </li><li><em>Qualitative Data Analysis</em> – A CITI Program Course - <a href='https://about.citiprogram.org/course/qualitative-data-analysis/'>https://about.citiprogram.org/course/qualitative-data-analysis/</a> </li><li><em>On Tech Ethics </em>– A CITI Program Podcast -  <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></description>
    <content:encoded><![CDATA[<p><b>What does meaningful child assent really look like in research?</b> In this episode of <em>On Research</em>, host Alexa McClellan speaks with Dr. David Coker about rethinking child assent beyond procedural compliance. Drawing on his recent scholarship, Dr. Coker explores gaps in current practices, regulatory tensions, inclusion of children with disabilities, and the role of IRBs in supporting assent as a developmentally appropriate, ethical process. The conversation challenges researchers to move from collecting assent as a formality to practicing it as a genuine expression of respect for children’s autonomy and voice. <br/> </p><p><b>Notes:</b> </p><ul><li>Coker, David C, Ketaki Inamdar, Daniel F. McCleary, and Lesley Cottrell.  2025. “Child Assent Practices in Research: Improving Ethics, Decision-Making, and Inclusivity.” <em>Journal of Educational Research &amp; Practice</em>. 15:1-24. <a href='https://files.eric.ed.gov/fulltext/EJ1492202.pdf'>https://files.eric.ed.gov/fulltext/EJ1492202.pdf</a> </li><li><em>Qualitative Data Analysis</em> – A CITI Program Course - <a href='https://about.citiprogram.org/course/qualitative-data-analysis/'>https://about.citiprogram.org/course/qualitative-data-analysis/</a> </li><li><em>On Tech Ethics </em>– A CITI Program Podcast -  <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></content:encoded>
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  <psc:chapter start="0:00" title="Rethinking Child Assent Practices - On Research Podcast" />
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  <psc:chapter start="0:40" title="Episode Introduction and Focus " />
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  <psc:chapter start="14:59" title="Power Dynamics and Ethical Responsibility " />
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  <psc:chapter start="33:55" title="Closing Reflections and Takeaways " />
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    <itunes:title>When Research Ends: Institutional Responsibility, Participant Protection, and Research Integrity - On Research Podcast</itunes:title>
    <title>When Research Ends: Institutional Responsibility, Participant Protection, and Research Integrity - On Research Podcast</title>
    <itunes:summary><![CDATA[When studies end abruptly, the ethical responsibilities don’t disappear. Dr. Brandon Brown joins host Alexa McClellan to examine institutional responsibility, participant protection, and research integrity when research is terminated unexpectedly—and what the end of a study reveals about trust in the research enterprise.    Notes:  Dr. Brandon Brown. “Your Study Is Terminated: Researchers Need to Prepare Participants.” The Hastings Center for Bioethics. November 19, 2025. ...]]></itunes:summary>
    <description><![CDATA[<p>When studies end abruptly, the ethical responsibilities don’t disappear. Dr. Brandon Brown joins host Alexa McClellan to examine institutional responsibility, participant protection, and research integrity when research is terminated unexpectedly—and what the end of a study reveals about trust in the research enterprise. <br/> </p><p><b>Notes:</b> </p><ul><li>Dr. Brandon Brown. “Your Study Is Terminated: Researchers Need to Prepare Participants.” <em>The Hastings Center for Bioethics</em>. November 19, 2025.  <a href='https://protect.checkpoint.com/v2/r01/___https:/www.thehastingscenter.org/your-study-is-terminated-researchers-need-to-prepare-participants/___.YzJ1OmNpdGlwcm9ncmFtMTpjOm86MTQ1ODdiZDBjOTdiOGExZDk1MzIxMDJjNWI0NzNhZjE6NzpjZTVhOmY4ZThmMDA0ZmJkNGFlN2U2OTE1MmY3NjNmYzgyOGFjODI0ZjRiN2Y1NzY5YzRiZDhmM2VmMjQ4ZmE4NDM4OGM6aDpUOkY'>https://www.thehastingscenter.org/your-study-is-terminated-researchers-need-to-prepare-participants/</a> </li><li><em>On Campus </em>– A CITI Program Podcast - <a href='https://protect.checkpoint.com/v2/r01/___https:/www.buzzsprout.com/1896915/___.YzJ1OmNpdGlwcm9ncmFtMTpjOm86MTQ1ODdiZDBjOTdiOGExZDk1MzIxMDJjNWI0NzNhZjE6Nzo4ZDliOjkwODdhOGQ0MmQ4MzhlZTc0MjQ2M2NmYTI4YTY0YjI5YTAzMzhiZDBlZDIzYmFiZGVkZTMxNThhNGYwNGZjODk6aDpUOkY'>https://www.buzzsprout.com/1896915/</a></li><li><em>Disaster Response and Research Reactivation</em> – A CITI Program Course - <a href='https://about.citiprogram.org/course/disaster-response-and-research-reactivation/'>https://about.citiprogram.org/course/disaster-response-and-research-reactivation/</a> </li><li>Dr. Brandon Brown’s CITI Program Author Page - <a href='https://about.citiprogram.org/authors/brandon-brown-mph-phd/'>https://about.citiprogram.org/authors/brandon-brown-mph-phd/</a>  </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a></li></ul>]]></description>
    <content:encoded><![CDATA[<p>When studies end abruptly, the ethical responsibilities don’t disappear. Dr. Brandon Brown joins host Alexa McClellan to examine institutional responsibility, participant protection, and research integrity when research is terminated unexpectedly—and what the end of a study reveals about trust in the research enterprise. <br/> </p><p><b>Notes:</b> </p><ul><li>Dr. Brandon Brown. “Your Study Is Terminated: Researchers Need to Prepare Participants.” <em>The Hastings Center for Bioethics</em>. November 19, 2025.  <a href='https://protect.checkpoint.com/v2/r01/___https:/www.thehastingscenter.org/your-study-is-terminated-researchers-need-to-prepare-participants/___.YzJ1OmNpdGlwcm9ncmFtMTpjOm86MTQ1ODdiZDBjOTdiOGExZDk1MzIxMDJjNWI0NzNhZjE6NzpjZTVhOmY4ZThmMDA0ZmJkNGFlN2U2OTE1MmY3NjNmYzgyOGFjODI0ZjRiN2Y1NzY5YzRiZDhmM2VmMjQ4ZmE4NDM4OGM6aDpUOkY'>https://www.thehastingscenter.org/your-study-is-terminated-researchers-need-to-prepare-participants/</a> </li><li><em>On Campus </em>– A CITI Program Podcast - <a href='https://protect.checkpoint.com/v2/r01/___https:/www.buzzsprout.com/1896915/___.YzJ1OmNpdGlwcm9ncmFtMTpjOm86MTQ1ODdiZDBjOTdiOGExZDk1MzIxMDJjNWI0NzNhZjE6Nzo4ZDliOjkwODdhOGQ0MmQ4MzhlZTc0MjQ2M2NmYTI4YTY0YjI5YTAzMzhiZDBlZDIzYmFiZGVkZTMxNThhNGYwNGZjODk6aDpUOkY'>https://www.buzzsprout.com/1896915/</a></li><li><em>Disaster Response and Research Reactivation</em> – A CITI Program Course - <a href='https://about.citiprogram.org/course/disaster-response-and-research-reactivation/'>https://about.citiprogram.org/course/disaster-response-and-research-reactivation/</a> </li><li>Dr. Brandon Brown’s CITI Program Author Page - <a href='https://about.citiprogram.org/authors/brandon-brown-mph-phd/'>https://about.citiprogram.org/authors/brandon-brown-mph-phd/</a>  </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a></li></ul>]]></content:encoded>
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  <psc:chapter start="0:00" title="When Research Ends: Institutional Responsibility, Participant Protection, and Research Integrity - On Research Podcast" />
  <psc:chapter start="0:20" title="Introduction and Episode Framing" />
  <psc:chapter start="0:49" title="Guest Introduction: Dr. Brandon Brown" />
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  <psc:chapter start="2:02" title="Why Study Termination Is a Blind Spot" />
  <psc:chapter start="4:17" title="Who Is Responsible When a Study Ends?" />
  <psc:chapter start="5:33" title="Funding Gaps and Ethical Obligations" />
  <psc:chapter start="7:36" title="Institutional Responsibility and Risk Management" />
  <psc:chapter start="8:12" title="What Participant Protection Looks Like at Termination" />
  <psc:chapter start="11:35" title="Consequences of Poorly Managed Terminations" />
  <psc:chapter start="14:19" title="On Campus Promo" />
  <psc:chapter start="14:42" title="Disproportionate Harm to Participants" />
  <psc:chapter start="18:04" title="Policy and Infrastructure Gaps" />
  <psc:chapter start="21:44" title="Similarity to Emergency Management" />
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  <psc:chapter start="27:50" title="Ethical Mandate to Proactively Address Terminations" />
  <psc:chapter start="28:35" title="Closing Remarks and Resources" />
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    <itunes:title>Opening Doors in STEM: Service Dogs, Advocacy, and Research Accessibility - On Research Podcast</itunes:title>
    <title>Opening Doors in STEM: Service Dogs, Advocacy, and Research Accessibility - On Research Podcast</title>
    <itunes:summary><![CDATA[In this episode of On Research, we explore how service dogs and advocacy are transforming accessibility for scientists with disability in STEM. Guests Joey Ramp-Adams and Madeline Jones share their lived experiences, discuss barriers in laboratory environments, and highlight how inclusive practices can create more equitable pathways in research.    Notes:  Sampsons Legacy Foundation - https://sampsonslegacyfoundation.com/  Working with Dogs in Research Settings – A CITI Pr...]]></itunes:summary>
    <description><![CDATA[<p>In this episode of <em>On Research</em>, we explore how service dogs and advocacy are transforming accessibility for scientists with disability in STEM. Guests Joey Ramp-Adams and Madeline Jones share their lived experiences, discuss barriers in laboratory environments, and highlight how inclusive practices can create more equitable pathways in research. <br/> </p><p><b>Notes:</b> </p><ul><li>Sampsons Legacy Foundation - <a href='https://sampsonslegacyfoundation.com/'>https://sampsonslegacyfoundation.com/</a>  </li><li><em>Working with Dogs in Research Settings –</em> A<em> </em>CITI Program course -  <a href='https://about.citiprogram.org/course/working-with-dogs-in-research-settings/'>https://about.citiprogram.org/course/working-with-dogs-in-research-settings/</a> </li><li><em>On Tech Ethics</em> – A CITI Program Podcast - <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></description>
    <content:encoded><![CDATA[<p>In this episode of <em>On Research</em>, we explore how service dogs and advocacy are transforming accessibility for scientists with disability in STEM. Guests Joey Ramp-Adams and Madeline Jones share their lived experiences, discuss barriers in laboratory environments, and highlight how inclusive practices can create more equitable pathways in research. <br/> </p><p><b>Notes:</b> </p><ul><li>Sampsons Legacy Foundation - <a href='https://sampsonslegacyfoundation.com/'>https://sampsonslegacyfoundation.com/</a>  </li><li><em>Working with Dogs in Research Settings –</em> A<em> </em>CITI Program course -  <a href='https://about.citiprogram.org/course/working-with-dogs-in-research-settings/'>https://about.citiprogram.org/course/working-with-dogs-in-research-settings/</a> </li><li><em>On Tech Ethics</em> – A CITI Program Podcast - <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></content:encoded>
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  <psc:chapter start="0:00" title="Opening Doors in STEM: Service Dogs, Advocacy, and Research Accessibility - On Research Podcast" />
  <psc:chapter start="0:01" title="Assumptions and Misconceptions About Service Dogs in Labs" />
  <psc:chapter start="1:04" title="Podcast Introduction and Episode Overview" />
  <psc:chapter start="2:44" title="Guest Introductions and Backgrounds" />
  <psc:chapter start="2:53" title="Joey’s Journey into Neuroscience and Advocacy" />
  <psc:chapter start="4:45" title="Madeline’s Path and Barriers Faced" />
  <psc:chapter start="9:27" title="Challenges in Lab Access and Institutional Responses" />
  <psc:chapter start="11:04" title="Joey’s Motivation for Advocacy and Policy Change" />
  <psc:chapter start="16:44" title="Barriers for Scientists with Disabilities" />
  <psc:chapter start="22:07" title="Common Misconceptions About Accommodations" />
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  <psc:chapter start="24:43" title="Policy Issues and CDC Guidelines " />
  <psc:chapter start="30:48" title="On Tech Ethics Promo" />
  <psc:chapter start="31:13" title="Mentorship’s Role in Accessibility" />
  <psc:chapter start="35:32" title="Samsons Legacy Foundation Initiatives" />
  <psc:chapter start="41:34" title="Impact of the Scholarship on Madeline" />
  <psc:chapter start="42:29" title="Visions for the Future of Accessibility in STEM" />
  <psc:chapter start="47:33" title="Episode Conclusion and Credits " />
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    <itunes:duration>2952</itunes:duration>
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    <itunes:title>Smart Tech, Smarter Questions: AI in Biomedical Research - On Research Podcast</itunes:title>
    <title>Smart Tech, Smarter Questions: AI in Biomedical Research - On Research Podcast</title>
    <itunes:summary><![CDATA[As artificial intelligence accelerates its influence on medicine and science, the real challenge is no longer whether AI is worth its cost—but how we choose to use it. In this episode, Dr. Catherine Bielick and Dr. Leo Anthony Celi examine how AI is transforming biomedical research and medical education, exposing deep flaws in legacy systems while offering a chance to rethink how knowledge is created, taught, and governed.    Notes:  On Campus – A CITI Program Podcast - https:/...]]></itunes:summary>
    <description><![CDATA[<p>As artificial intelligence accelerates its influence on medicine and science, the real challenge is no longer whether AI is worth its cost—but how we choose to use it. In this episode, Dr. Catherine Bielick and Dr. Leo Anthony Celi examine how AI is transforming biomedical research and medical education, exposing deep flaws in legacy systems while offering a chance to rethink how knowledge is created, taught, and governed. <br/> </p><p><b>Notes:</b> </p><ul><li><em>On Campus</em> – A CITI Program Podcast - <a href='https://www.buzzsprout.com/1896915/'>https://www.buzzsprout.com/1896915/</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></description>
    <content:encoded><![CDATA[<p>As artificial intelligence accelerates its influence on medicine and science, the real challenge is no longer whether AI is worth its cost—but how we choose to use it. In this episode, Dr. Catherine Bielick and Dr. Leo Anthony Celi examine how AI is transforming biomedical research and medical education, exposing deep flaws in legacy systems while offering a chance to rethink how knowledge is created, taught, and governed. <br/> </p><p><b>Notes:</b> </p><ul><li><em>On Campus</em> – A CITI Program Podcast - <a href='https://www.buzzsprout.com/1896915/'>https://www.buzzsprout.com/1896915/</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></content:encoded>
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    <pubDate>Tue, 23 Dec 2025 11:00:00 -0500</pubDate>
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  <psc:chapter start="0:00" title="Smart Tech, Smarter Questions: AI in Biomedical Research - On Research Podcast" />
  <psc:chapter start="0:01" title="AI’s Inevitable Role in Science" />
  <psc:chapter start="0:43" title="Podcast Introduction &amp; Episode Overview" />
  <psc:chapter start="2:10" title="Guest Introductions" />
  <psc:chapter start="2:55" title="AI’s Impact on Research &amp; Education" />
  <psc:chapter start="4:48" title="Risks of AI-Generated Science" />
  <psc:chapter start="7:39" title="Overhauling Medical Knowledge Systems" />
  <psc:chapter start="9:18" title="Where’s the Harm? AI as Tool and Risk" />
  <psc:chapter start="11:44" title="AI, Cheating, and Medical Education" />
  <psc:chapter start="13:47" title="External Incentives and Publish-or-Perish" />
  <psc:chapter start="16:32" title="AI as Fire: Opportunity and Threat" />
  <psc:chapter start="16:51" title="Rethinking Education: Teaching Thinking, Not Facts" />
  <psc:chapter start="17:35" title="Challenges of Integrating AI in Medical Education" />
  <psc:chapter start="19:22" title="On Campus Promo" />
  <psc:chapter start="19:48" title="Why Traditional Approaches Fall Short" />
  <psc:chapter start="23:47" title="Critical Thinking Through Diverse Collaboration" />
  <psc:chapter start="26:06" title="Core Competencies Over Cutting-Edge Features" />
  <psc:chapter start="27:18" title="Designing Human-AI Systems for Virtue" />
  <psc:chapter start="28:55" title="The Pace of AI and Outdated Curricula" />
  <psc:chapter start="31:29" title="Who Should Shape the Future?" />
  <psc:chapter start="32:03" title="Science, Politics, and Advocacy" />
  <psc:chapter start="33:12" title="Ensuring Transparency and Integrity in AI Research" />
  <psc:chapter start="36:21" title="Practical AI Literacy for All" />
  <psc:chapter start="38:00" title="Future-Proofing Research Behavior, Not Just Metrics" />
  <psc:chapter start="39:54" title="Learning from History: Redesigning for the AI Era" />
  <psc:chapter start="41:07" title="Episode Conclusion &amp; Credits" />
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    <itunes:title>2025 PRIM&amp;R Annual Conference Roundup - On Research Podcast</itunes:title>
    <title>2025 PRIM&amp;R Annual Conference Roundup - On Research Podcast</title>
    <itunes:summary><![CDATA[In this episode of On Research, we talk with attendees, presenters, and exhibitors who were at the 2025 PRIM&amp;R Annual Conference in Baltimore about key takeaways, emerging themes, and what this year’s conference reveals about where research and ethics compliance is headed next.    Notes:  PRIM&amp;R   - https://primr.org/ On Tech Ethics – A CITI Program Podcast - https://www.buzzsprout.com/2120643 CITI Program’s course catalog: https://about.citiprogram.org/c...]]></itunes:summary>
    <description><![CDATA[<p>In this episode of <em>On Research</em>, we talk with attendees, presenters, and exhibitors who were at the 2025 PRIM&amp;R Annual Conference in Baltimore about key takeaways, emerging themes, and what this year’s conference reveals about where research and ethics compliance is headed next. <br/> </p><p><b>Notes:</b> </p><ul><li>PRIM&amp;R   - <a href='https://primr.org/'>https://primr.org/</a> </li><li><em>On Tech Ethics</em> – A CITI Program Podcast - <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul><p> </p>]]></description>
    <content:encoded><![CDATA[<p>In this episode of <em>On Research</em>, we talk with attendees, presenters, and exhibitors who were at the 2025 PRIM&amp;R Annual Conference in Baltimore about key takeaways, emerging themes, and what this year’s conference reveals about where research and ethics compliance is headed next. <br/> </p><p><b>Notes:</b> </p><ul><li>PRIM&amp;R   - <a href='https://primr.org/'>https://primr.org/</a> </li><li><em>On Tech Ethics</em> – A CITI Program Podcast - <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul><p> </p>]]></content:encoded>
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    <itunes:author>CITI Program</itunes:author>
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    <pubDate>Tue, 25 Nov 2025 09:00:00 -0500</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="2025 PRIM&amp;R Annual Conference Roundup - On Research Podcast" />
  <psc:chapter start="0:03" title="Opening Reflections on Community" />
  <psc:chapter start="0:52" title="Podcast Introduction &amp; Episode Overview" />
  <psc:chapter start="1:30" title="Panel Introductions" />
  <psc:chapter start="2:20" title="Major Takeaways: AI and Community" />
  <psc:chapter start="4:00" title="Exhibit Hall Perspectives" />
  <psc:chapter start="5:10" title="Interactions with Attendees" />
  <psc:chapter start="6:01" title="Common Challenges Across Communities" />
  <psc:chapter start="7:38" title="Emerging Themes: Discontinuation &amp; Dedication" />
  <psc:chapter start="9:04" title="Balancing Hope and Anxiety" />
  <psc:chapter start="9:50" title="On Tech Ethics Promo" />
  <psc:chapter start="10:14" title="Future Directions: AI and Frameworks" />
  <psc:chapter start="11:26" title="AI in Auditing and Funding Shifts" />
  <psc:chapter start="12:31" title="Practical Adjustments for Funding" />
  <psc:chapter start="13:07" title="AI as Tool and Challenge" />
  <psc:chapter start="13:57" title="Expanding Training on AI " />
  <psc:chapter start="14:26" title="Practical Takeaways for Programs" />
  <psc:chapter start="15:46" title="Data Integrity and Survey Fraud" />
  <psc:chapter start="17:20" title="Compliance and Process Improvements" />
  <psc:chapter start="18:23" title="Attendee Reactions: Collaboration &amp; Support" />
  <psc:chapter start="19:34" title="Attendee Reactions: Community &amp; Innovation" />
  <psc:chapter start="21:52" title="Attendee Reactions: Data Integrity" />
  <psc:chapter start="22:41" title="Attendee Reactions: The Power of Gathering" />
  <psc:chapter start="24:16" title="Keynote Reflections: Shared Purpose" />
  <psc:chapter start="25:28" title="Exhibitor Presence and Consistency" />
  <psc:chapter start="26:12" title="In-Person Connection Value" />
  <psc:chapter start="27:08" title="Poster Presentations and Compliance" />
  <psc:chapter start="28:15" title="Affirming Training Needs" />
  <psc:chapter start="29:43" title="Keeping Up with Regulatory Changes" />
  <psc:chapter start="30:23" title="Closing Remarks and Credits" />
</psc:chapters>
    <itunes:duration>1911</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>11</itunes:episode>
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  <item>
    <itunes:title>Ethics, Innovation, and the Future of Animal Research - On Research Podcast</itunes:title>
    <title>Ethics, Innovation, and the Future of Animal Research - On Research Podcast</title>
    <itunes:summary><![CDATA[In this episode of On Research, we talk with Dr. Megan LaFollette, Executive Director of the 3Rs Collaborative, about the practical applications of Replacement, Reduction, and Refinement, emerging animal model alternatives, and how federal initiatives are shaping the future of science.      Notes:  The 3Rs Collaborative:  https://3rc.org/ The 3Rs Certificate Course: https://about.citiprogram.org/course/3rs-certificate-course/ On Campus – A CITI Program Podca...]]></itunes:summary>
    <description><![CDATA[<p>In this episode of <em>On Research</em>, we talk with Dr. Megan LaFollette, Executive Director of the 3Rs Collaborative, about the practical applications of Replacement, Reduction, and Refinement, emerging animal model alternatives, and how federal initiatives are shaping the future of science.   <br/> </p><p><b>Notes:</b> </p><ul><li>The 3Rs Collaborative:  <a href='https://3rc.org/'>https://3rc.org/</a> </li><li>The <em>3Rs Certificate Course</em>: <a href='https://about.citiprogram.org/course/3rs-certificate-course/'>https://about.citiprogram.org/course/3rs-certificate-course/ </a></li><li><em>On Campus</em> – A CITI Program Podcast: <a href='https://www.buzzsprout.com/1896915/'>https://www.buzzsprout.com/1896915/</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></description>
    <content:encoded><![CDATA[<p>In this episode of <em>On Research</em>, we talk with Dr. Megan LaFollette, Executive Director of the 3Rs Collaborative, about the practical applications of Replacement, Reduction, and Refinement, emerging animal model alternatives, and how federal initiatives are shaping the future of science.   <br/> </p><p><b>Notes:</b> </p><ul><li>The 3Rs Collaborative:  <a href='https://3rc.org/'>https://3rc.org/</a> </li><li>The <em>3Rs Certificate Course</em>: <a href='https://about.citiprogram.org/course/3rs-certificate-course/'>https://about.citiprogram.org/course/3rs-certificate-course/ </a></li><li><em>On Campus</em> – A CITI Program Podcast: <a href='https://www.buzzsprout.com/1896915/'>https://www.buzzsprout.com/1896915/</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul>]]></content:encoded>
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    <pubDate>Tue, 28 Oct 2025 11:00:00 -0400</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Promise and Limitations of New Approach Methods" />
  <psc:chapter start="0:27" title="Introduction and Overview" />
  <psc:chapter start="1:19" title="Dr. LaFollette’s Background" />
  <psc:chapter start="3:16" title="Mission of the Three R’s Collaborative" />
  <psc:chapter start="4:16" title="Three R’s Collaborative Initiatives" />
  <psc:chapter start="7:01" title="Balancing Ethics and Scientific Rigor" />
  <psc:chapter start="8:59" title="Promise of New Approach Methods" />
  <psc:chapter start="11:17" title="Limitations and Gaps in NAMs" />
  <psc:chapter start="15:00" title="Federal Initiatives and Priorities" />
  <psc:chapter start="17:46" title="Impact of Federal Funding on NAM Adoption" />
  <psc:chapter start="19:02" title="Collaboration Across Sectors" />
  <psc:chapter start="22:10" title="Reduction and Refinement in Practice" />
  <psc:chapter start="26:55" title="Advice for Early Career Scientists" />
  <psc:chapter start="29:17" title="Closing Remarks and Resources" />
</psc:chapters>
    <itunes:duration>1855</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>10</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
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  <item>
    <itunes:title>Black Women in Clinical Research: Building Community and Breaking Barriers - On Research Podcast</itunes:title>
    <title>Black Women in Clinical Research: Building Community and Breaking Barriers - On Research Podcast</title>
    <itunes:summary><![CDATA[In this episode, we talk with Danielle Mitchell, CEO and founder of Black Women in Clinical Research (BWICR), a professional organization dedicated to empowering, supporting, and connecting Black women working in clinical research through mentorship, networking, and career development opportunities.    Notes:  Black Women in Clinical Research (BWICR) - https://bwicr.com/ On Tech Ethics – A CITI Program Podcast: https://www.buzzsprout.com/2120643 CITI Program’s course ...]]></itunes:summary>
    <description><![CDATA[<p>In this episode, we talk with Danielle Mitchell, CEO and founder of Black Women in Clinical Research (BWICR), a professional organization dedicated to empowering, supporting, and connecting Black women working in clinical research through mentorship, networking, and career development opportunities. <br/> </p><p><b>Notes:</b> </p><ul><li>Black Women in Clinical Research (BWICR) - <a href='https://bwicr.com/'>https://bwicr.com/</a> </li><li><em>On Tech Ethics</em> – A CITI Program Podcast: <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul><p> </p>]]></description>
    <content:encoded><![CDATA[<p>In this episode, we talk with Danielle Mitchell, CEO and founder of Black Women in Clinical Research (BWICR), a professional organization dedicated to empowering, supporting, and connecting Black women working in clinical research through mentorship, networking, and career development opportunities. <br/> </p><p><b>Notes:</b> </p><ul><li>Black Women in Clinical Research (BWICR) - <a href='https://bwicr.com/'>https://bwicr.com/</a> </li><li><em>On Tech Ethics</em> – A CITI Program Podcast: <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li><li>CITI Program’s course catalog: <a href='https://about.citiprogram.org/course-catalog'>https://about.citiprogram.org/course-catalog </a> </li></ul><p> </p>]]></content:encoded>
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    <pubDate>Tue, 30 Sep 2025 11:00:00 -0400</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Black Women in Clinical Research: Building Community and Breaking Barriers - On Research Podcast" />
  <psc:chapter start="0:12" title="Introduction and Guest Background" />
  <psc:chapter start="1:25" title="Danielle’s Personal Journey into Clinical Research" />
  <psc:chapter start="2:30" title="Discovering Clinical Research and Early Barriers" />
  <psc:chapter start="4:38" title="First Clinical Research Role and Continued Challenges" />
  <psc:chapter start="5:36" title="Founding Black Women in Clinical Research (BWICR)" />
  <psc:chapter start="7:39" title="BWICR’s Support Systems and Resources" />
  <psc:chapter start="10:18" title="BWICR Conference Overview" />
  <psc:chapter start="12:54" title="Conference Logistics and Registration" />
  <psc:chapter start="13:44" title="On Tech Podcast Commercial" />
  <psc:chapter start="14:12" title="Mentorship in BWICR" />
  <psc:chapter start="18:36" title="Mentorship Success Story" />
  <psc:chapter start="20:57" title="Barriers Faced by Black Women in Clinical Research" />
  <psc:chapter start="22:43" title="Importance of Diverse Voices in Research" />
  <psc:chapter start="25:02" title="Future Initiatives and Goals for BWICR" />
  <psc:chapter start="26:53" title="Advice for Aspiring Clinical Research Professionals" />
  <psc:chapter start="28:43" title="How to Connect with BWICR" />
  <psc:chapter start="29:50" title="Closing Remarks and Additional Resources" />
</psc:chapters>
    <itunes:duration>1887</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>9</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>The NIH Mandate for Posting IBC Minutes: Guidance for Institutions - On Research Podcast</itunes:title>
    <title>The NIH Mandate for Posting IBC Minutes: Guidance for Institutions - On Research Podcast</title>
    <itunes:summary><![CDATA[Guest host Dr. Anne Hawkinsbadge (CITI Program) and Dr. Regina Allen (Virginia Tech) discuss the NIH’s new requirement for Institutional Biosafety Committees (IBCs) to post approved meeting minutes online, effective June 1. They explore how institutions can comply, while also examining the role, membership, and importance of IBCs in research compliance and safety.     Notes:  National Institutes of Health (NIH) “NOT-OD-25-082: Implementation Update: Promoting Maximal Transparen...]]></itunes:summary>
    <description><![CDATA[<p>Guest host Dr. Anne Hawkinsbadge (CITI Program) and Dr. Regina Allen (Virginia Tech) discuss the NIH’s new requirement for Institutional Biosafety Committees (IBCs) to post approved meeting minutes online, effective June 1. They explore how institutions can comply, while also examining the role, membership, and importance of IBCs in research compliance and safety. <br/> <br/><br/>Notes: </p><ul><li>National Institutes of Health (NIH) “NOT-OD-25-082: Implementation Update: Promoting Maximal Transparency Under the NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules” <a href='https://grants.nih.gov/grants/guide/notice-files/NOT-OD-25-082.html'>https://grants.nih.gov/grants/guide/notice-files/NOT-OD-25-082.html</a></li><li>On Campus – A CITI Program Podcast: <a href='https://www.buzzsprout.com/1896915'>https://www.buzzsprout.com/1896915</a> </li><li>CITI Program – Biosafety and Biosecurity Course Catalog <a href='https://about.citiprogram.org/courses/?fwp_series=242&amp;fwp_sort_courses=popularity '>https://about.citiprogram.org/courses/?fwp_series=242&amp;fwp_sort_courses=popularity </a></li></ul>]]></description>
    <content:encoded><![CDATA[<p>Guest host Dr. Anne Hawkinsbadge (CITI Program) and Dr. Regina Allen (Virginia Tech) discuss the NIH’s new requirement for Institutional Biosafety Committees (IBCs) to post approved meeting minutes online, effective June 1. They explore how institutions can comply, while also examining the role, membership, and importance of IBCs in research compliance and safety. <br/> <br/><br/>Notes: </p><ul><li>National Institutes of Health (NIH) “NOT-OD-25-082: Implementation Update: Promoting Maximal Transparency Under the NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules” <a href='https://grants.nih.gov/grants/guide/notice-files/NOT-OD-25-082.html'>https://grants.nih.gov/grants/guide/notice-files/NOT-OD-25-082.html</a></li><li>On Campus – A CITI Program Podcast: <a href='https://www.buzzsprout.com/1896915'>https://www.buzzsprout.com/1896915</a> </li><li>CITI Program – Biosafety and Biosecurity Course Catalog <a href='https://about.citiprogram.org/courses/?fwp_series=242&amp;fwp_sort_courses=popularity '>https://about.citiprogram.org/courses/?fwp_series=242&amp;fwp_sort_courses=popularity </a></li></ul>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/2112707/episodes/17736177-the-nih-mandate-for-posting-ibc-minutes-guidance-for-institutions-on-research-podcast.mp3" length="27905418" type="audio/mpeg" />
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    <pubDate>Tue, 26 Aug 2025 10:00:00 -0400</pubDate>
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  <psc:chapter start="0:00" title="The NIH Mandate for Posting IBC Minutes: Guidance for Institutions - On Research Podcast" />
  <psc:chapter start="0:34" title="Podcast Introduction and Episode Overview" />
  <psc:chapter start="1:59" title="Dr. Anne Hawkinsbadge interviews Dr. Regina Allen" />
  <psc:chapter start="5:19" title="Transition to NIH Mandate Discussion" />
  <psc:chapter start="5:45" title="When IBC Committees Are Required" />
  <psc:chapter start="6:30" title="Definitions: Recombinant and Synthetic Nucleic Acids" />
  <psc:chapter start="8:00" title="Definition of Institution and IBC Role" />
  <psc:chapter start="9:16" title="NIH Expectations for IBC Committees" />
  <psc:chapter start="12:39" title="Importance of Diverse IBC Membership" />
  <psc:chapter start="14:04" title="Role of Community Members and Transparency " />
  <psc:chapter start="15:31" title="History of IBC Minutes Access and New Posting Requirement" />
  <psc:chapter start="17:50" title="Transition to Written Procedures for Minutes" />
  <psc:chapter start="19:00" title="On Campus Commercial" />
  <psc:chapter start="23:15" title="Redaction of Sensitive Information from Minutes " />
  <psc:chapter start="27:18" title="Security and Stakeholder Notification" />
  <psc:chapter start="28:56" title="Risk Assessment and Monitoring Public Access" />
  <psc:chapter start="32:18" title="Retention Period for Posted Minutes" />
  <psc:chapter start="33:26" title="Auditing and Record-Keeping Plans" />
  <psc:chapter start="34:47" title="Final Reflections and Benefits of the New Policy (" />
  <psc:chapter start="37:12" title="Podcast Closing and Additional Resources" />
</psc:chapters>
    <itunes:duration>2322</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>8</itunes:episode>
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  <item>
    <itunes:title>Navigating the Ethics of Insect Research: Sentience, Welfare, and Scientific Responsibility - On Research Podcast</itunes:title>
    <title>Navigating the Ethics of Insect Research: Sentience, Welfare, and Scientific Responsibility - On Research Podcast</title>
    <itunes:summary><![CDATA[They outnumber us by the quintillions. They’re used in research across genetics, behavior, ecology, neuroscience—even robotics. But when it comes to ethics and welfare, insects are often left out of the conversation. Can they feel pain? What responsibilities do researchers have to them? This episode of On Research explores big ethical questions about our smallest research subjects. Our guests are Dr. Meghan Barrett (Indiana University Indianapolis) and Dr. Bob Fischer (Texas State University)...]]></itunes:summary>
    <description><![CDATA[<p>They outnumber us by the quintillions. They’re used in research across genetics, behavior, ecology, neuroscience—even robotics. But when it comes to ethics and welfare, insects are often left out of the conversation. Can they feel pain? What responsibilities do researchers have to them? This episode of <em>On Research</em> explores big ethical questions about our smallest research subjects. Our guests are Dr. Meghan Barrett (Indiana University Indianapolis) and Dr. Bob Fischer (Texas State University), co-founders of the Insect Welfare Research Society. </p><p>For links to studies, references, and further reading, please visit the CITI Program blog - <a href='https://about.citiprogram.org/blog/on-research-podcast-navigating-the-ethics-of-insect-research-sentience-welfare-and-scientific-responsibility/'>https://about.citiprogram.org/blog/on-research-podcast-navigating-the-ethics-of-insect-research-sentience-welfare-and-scientific-responsibility/</a></p><p><b>Notes:</b> </p><ul><li>Clarification at 14:32 by Barrett: There are direct connections between sensory integrative brain regions and connections from the nociceptors to the sensory integrative brain regions (but that these are, necessarily, not direct.) </li><li>Consistent with the Indiana University Statement of Policy on Institutional Neutrality, the comments by Barrett contained in this communication are solely her own and such comments and content are not intended to be construed, and shall not be construed, as the views of Indiana University or comments made on behalf of or by Indiana University. </li></ul><p>Additional resources:</p><ul><li><em>Working with Insects in Research Settings – </em>A CITI Program Course <a href='https://about.citiprogram.org/course/working-with-insects-in-research-settings/'>https://about.citiprogram.org/course/working-with-insects-in-research-settings/</a> </li><li><em>On Tech Ethics</em> – A CITI Program Podcast: <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li></ul><p><br/></p>]]></description>
    <content:encoded><![CDATA[<p>They outnumber us by the quintillions. They’re used in research across genetics, behavior, ecology, neuroscience—even robotics. But when it comes to ethics and welfare, insects are often left out of the conversation. Can they feel pain? What responsibilities do researchers have to them? This episode of <em>On Research</em> explores big ethical questions about our smallest research subjects. Our guests are Dr. Meghan Barrett (Indiana University Indianapolis) and Dr. Bob Fischer (Texas State University), co-founders of the Insect Welfare Research Society. </p><p>For links to studies, references, and further reading, please visit the CITI Program blog - <a href='https://about.citiprogram.org/blog/on-research-podcast-navigating-the-ethics-of-insect-research-sentience-welfare-and-scientific-responsibility/'>https://about.citiprogram.org/blog/on-research-podcast-navigating-the-ethics-of-insect-research-sentience-welfare-and-scientific-responsibility/</a></p><p><b>Notes:</b> </p><ul><li>Clarification at 14:32 by Barrett: There are direct connections between sensory integrative brain regions and connections from the nociceptors to the sensory integrative brain regions (but that these are, necessarily, not direct.) </li><li>Consistent with the Indiana University Statement of Policy on Institutional Neutrality, the comments by Barrett contained in this communication are solely her own and such comments and content are not intended to be construed, and shall not be construed, as the views of Indiana University or comments made on behalf of or by Indiana University. </li></ul><p>Additional resources:</p><ul><li><em>Working with Insects in Research Settings – </em>A CITI Program Course <a href='https://about.citiprogram.org/course/working-with-insects-in-research-settings/'>https://about.citiprogram.org/course/working-with-insects-in-research-settings/</a> </li><li><em>On Tech Ethics</em> – A CITI Program Podcast: <a href='https://www.buzzsprout.com/2120643'>https://www.buzzsprout.com/2120643</a> </li></ul><p><br/></p>]]></content:encoded>
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    <pubDate>Tue, 29 Jul 2025 11:00:00 -0400</pubDate>
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  <psc:chapter start="0:00" title="Navigating the Ethics of Insect Research: Sentience, Welfare, and Scientific Responsibility - On Research Podcast" />
  <psc:chapter start="0:01" title="Opening Reflections on Sentience Evidence" />
  <psc:chapter start="0:36" title="Podcast Introduction &amp; Episode Overview" />
  <psc:chapter start="1:22" title="Guest Introductions &amp; Backgrounds " />
  <psc:chapter start="4:11" title="How Insects Are Used in Research" />
  <psc:chapter start="6:43" title="Defining Sentience &amp; Assessing It in Animals " />
  <psc:chapter start="12:00" title="Applying Sentience Frameworks to Insects " />
  <psc:chapter start="13:54" title="Evidence for Insect Sentience &amp; Precautionary Standards " />
  <psc:chapter start="18:20" title="Ethical Considerations &amp; Instrumental Reasons for Insect Welfare " />
  <psc:chapter start="22:03" title="Minimizing Harm in Insect Research " />
  <psc:chapter start="25:25" title="Applying Vertebrate Animal Welfare Principles to Insects " />
  <psc:chapter start="28:36" title="PI and Research Team Responsibilities " />
  <psc:chapter start="31:41" title="Institutional Norms, Public Trust, and Policy " />
  <psc:chapter start="34:36" title="Future Directions: Community Dialogue &amp; Best Practices " />
  <psc:chapter start="36:17" title="Future Directions: Evidence Gathering &amp; Research Needs " />
  <psc:chapter start="37:26" title="Closing Remarks &amp; Podcast Outro " />
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    <itunes:duration>2328</itunes:duration>
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    <itunes:episode>7</itunes:episode>
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    <itunes:title>Building Trust in Science: The Essential Role of Research Integrity Officers - On Research Podcast</itunes:title>
    <title>Building Trust in Science: The Essential Role of Research Integrity Officers - On Research Podcast</title>
    <itunes:summary><![CDATA[Today we’re stepping behind the scenes into a critical – but often invisible – part of the research world: maintaining integrity. Joining us is Dr. Courtney Karmelita, Executive Director of Ethical Research and Outreach at Penn State. In today's conversation, we'll talk about what really happens when concerns are raised, how institutions handle research misconduct investigations, the challenges of navigating gray areas, and why a culture of integrity matters now more than ever.     ...]]></itunes:summary>
    <description><![CDATA[<p>Today we’re stepping behind the scenes into a critical – but often invisible – part of the research world: maintaining integrity. Joining us is Dr. Courtney Karmelita, Executive Director of Ethical Research and Outreach at Penn State. In today&apos;s conversation, we&apos;ll talk about what really happens when concerns are raised, how institutions handle research misconduct investigations, the challenges of navigating gray areas, and why a culture of integrity matters now more than ever.<em> </em> <br/> </p><p>Additional resources: </p><ul><li><b>Interested in learning more about research integrity? Register for CITI Program’s free live webinar “I’m a new RIO, what do I do now?” on July 9</b>. <a href='https://about.citiprogram.org/news/free-live-webinar-im-a-new-rio-what-do-i-do-now/'>https://about.citiprogram.org/news/free-live-webinar-im-a-new-rio-what-do-i-do-now/</a> </li><li><b><em>On Campus</em></b> <b>– A CITI Program Podcast</b>: <a href='https://www.buzzsprout.com/1896915/'>https://www.buzzsprout.com/1896915/</a> </li><li><b>CITI Program Course Catalog:</b> <a href='https://about.citiprogram.org/courses/'>https://about.citiprogram.org/courses/</a> </li></ul>]]></description>
    <content:encoded><![CDATA[<p>Today we’re stepping behind the scenes into a critical – but often invisible – part of the research world: maintaining integrity. Joining us is Dr. Courtney Karmelita, Executive Director of Ethical Research and Outreach at Penn State. In today&apos;s conversation, we&apos;ll talk about what really happens when concerns are raised, how institutions handle research misconduct investigations, the challenges of navigating gray areas, and why a culture of integrity matters now more than ever.<em> </em> <br/> </p><p>Additional resources: </p><ul><li><b>Interested in learning more about research integrity? Register for CITI Program’s free live webinar “I’m a new RIO, what do I do now?” on July 9</b>. <a href='https://about.citiprogram.org/news/free-live-webinar-im-a-new-rio-what-do-i-do-now/'>https://about.citiprogram.org/news/free-live-webinar-im-a-new-rio-what-do-i-do-now/</a> </li><li><b><em>On Campus</em></b> <b>– A CITI Program Podcast</b>: <a href='https://www.buzzsprout.com/1896915/'>https://www.buzzsprout.com/1896915/</a> </li><li><b>CITI Program Course Catalog:</b> <a href='https://about.citiprogram.org/courses/'>https://about.citiprogram.org/courses/</a> </li></ul>]]></content:encoded>
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  <psc:chapter start="0:00" title="Building Trust in Science: The Essential Role of Research Integrity Officers - On Research Podcast" />
  <psc:chapter start="0:22" title="Introduction and Guest Background" />
  <psc:chapter start="1:43" title="Dr. Karmelita’s Role as Research Integrity Officer" />
  <psc:chapter start="5:31" title="Path to Research Integrity" />
  <psc:chapter start="9:00" title="A Typical Day in the RIO’s Office" />
  <psc:chapter start="11:34" title="Balancing Education and Investigation" />
  <psc:chapter start="14:03" title="Common Cases and Issues" />
  <psc:chapter start="16:39" title="Handling Research Misconduct Allegations" />
  <psc:chapter start="19:01" title="Navigating Ethical Gray Areas" />
  <psc:chapter start="21:16" title="Addressing Weaponization of the Process" />
  <psc:chapter start="22:36" title="Dealing with Unclear Situations" />
  <psc:chapter start="24:16" title="Developing Helpful Tools and the Challenge of Discerning Intent " />
  <psc:chapter start="26:33" title="Changes in the Research Integrity Landscape" />
  <psc:chapter start="29:12" title="Building a Culture of Ethics and Compliance" />
  <psc:chapter start="33:15" title="Collaboration with External Bodies" />
  <psc:chapter start="35:08" title="Emerging Issues and Trends" />
  <psc:chapter start="37:36" title="Misconceptions About the RIO Role" />
  <psc:chapter start="39:36" title="Advice for Aspiring Research Integrity Professionals" />
  <psc:chapter start="40:12" title="Closing and Podcast Information" />
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    <itunes:duration>2523</itunes:duration>
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  <item>
    <itunes:title>Engaging with Online Communities: Ethical Considerations for Researchers - On Research Podcast</itunes:title>
    <title>Engaging with Online Communities: Ethical Considerations for Researchers - On Research Podcast</title>
    <itunes:summary><![CDATA[How do we responsibly study digital communities without violating their trust? Where do we draw the line between research and interference? Joining us today is Dr. Sarah Gilbert, a research associate at Cornell University and research director of the Citizens and Technology Lab. Her work focuses on supporting healthy online communities, including how online data can be reused ethically. Together, we'll unpack the CMV subreddit case, explore how current research norms are being tested in real ...]]></itunes:summary>
    <description><![CDATA[<p>How do we responsibly study digital communities without violating their trust? Where do we draw the line between research and interference? Joining us today is Dr. Sarah Gilbert, a research associate at Cornell University and research director of the Citizens and Technology Lab. Her work focuses on supporting healthy online communities, including how online data can be reused ethically. Together, we&apos;ll unpack the CMV subreddit case, explore how current research norms are being tested in real time, and ask what a more transparent future might look like.  <br/><br/></p><p><b>Additional resources:</b>  </p><p>Research papers about ethical research on Reddit: </p><ul><li><a href='https://dl.acm.org/doi/abs/10.1145/3633070'>Remember the Human: A Systematic Review of Ethical Considerations in Reddit Research</a> - https://dl.acm.org/doi/abs/10.1145/3633070</li><li><a href='https://journals.sagepub.com/doi/full/10.1177/20539517231164108'>Cross-Platform user expectations for social media data reuse</a> - https://journals.sagepub.com/doi/full/10.1177/20539517231164108</li></ul><p>Guides: </p><ul><li><a href='https://linkprotect.cudasvc.com/url?a=https%3a%2f%2faoir.org%2fethics%2f&amp;c=E,1,OnzDF3IU-1DBKVIKRKmqHEto0suKPCRNtw95j74fcvEfF4NX04i5ds_MM50WXDyN-QlgJPjPM445BfKdCJvwm4raRKysQFXNUncKQgYwncrslcDjL-nl&amp;typo=1'>Association for Internet Researchers: </a><a href='https://linkprotect.cudasvc.com/url?a=https%3a%2f%2faoir.org%2fethics%2f&amp;c=E,1,6x_FqIN3L3lBg-wPwDn7aTxTNzIpA_cnOCtYltTA891hYy3jD_t0pgkRt3-H-OoGJ5tb5GRBNxrlb9SxV6LwYjsCR96x61B63YQbbPbmtoNsdtl8oW0,&amp;typo=1'>Internet Research: Ethical Guidelines 3.0</a> - https://aoir.org/ethics/ </li><li><a href='https://pervade.umd.edu/pervade-data-ethics-tool/'>PERVADE Data Ethics Tool</a> - https://pervade.umd.edu/pervade-data-ethics-tool/</li><li><a href='https://www.reddit.com/r/AskHistorians/comments/1iu4otk/meta_new_policy_for_researchers_using/'>AskHistorians Policy for Researchers using r/AskHistorians in Research</a> - https://www.reddit.com/r/AskHistorians/comments/1iu4otk/meta_new_policy_for_researchers_using/</li><li><a href='https://journals.sagepub.com/doi/full/10.1177/20539517211040759'>Excavating awareness and power in data science: A manifesto for trustworthy pervasive data research</a> - https://journals.sagepub.com/doi/full/10.1177/20539517211040759</li><li><a href='https://arxiv.org/pdf/2503.13752'>Beyond the Individual: A Community-Engaged Framework for Ethical Online Community Research</a> - https://arxiv.org/pdf/2503.13752</li></ul><p>Tool for large-scale disclosure: </p><ul><li><a href='https://journals.sagepub.com/doi/10.1177/20563051221077021'>Procedural and Substantive Ethics in the Design of Research Ethics Systems</a> - https://journals.sagepub.com/doi/10.1177/20563051221077021</li></ul><p> </p>]]></description>
    <content:encoded><![CDATA[<p>How do we responsibly study digital communities without violating their trust? Where do we draw the line between research and interference? Joining us today is Dr. Sarah Gilbert, a research associate at Cornell University and research director of the Citizens and Technology Lab. Her work focuses on supporting healthy online communities, including how online data can be reused ethically. Together, we&apos;ll unpack the CMV subreddit case, explore how current research norms are being tested in real time, and ask what a more transparent future might look like.  <br/><br/></p><p><b>Additional resources:</b>  </p><p>Research papers about ethical research on Reddit: </p><ul><li><a href='https://dl.acm.org/doi/abs/10.1145/3633070'>Remember the Human: A Systematic Review of Ethical Considerations in Reddit Research</a> - https://dl.acm.org/doi/abs/10.1145/3633070</li><li><a href='https://journals.sagepub.com/doi/full/10.1177/20539517231164108'>Cross-Platform user expectations for social media data reuse</a> - https://journals.sagepub.com/doi/full/10.1177/20539517231164108</li></ul><p>Guides: </p><ul><li><a href='https://linkprotect.cudasvc.com/url?a=https%3a%2f%2faoir.org%2fethics%2f&amp;c=E,1,OnzDF3IU-1DBKVIKRKmqHEto0suKPCRNtw95j74fcvEfF4NX04i5ds_MM50WXDyN-QlgJPjPM445BfKdCJvwm4raRKysQFXNUncKQgYwncrslcDjL-nl&amp;typo=1'>Association for Internet Researchers: </a><a href='https://linkprotect.cudasvc.com/url?a=https%3a%2f%2faoir.org%2fethics%2f&amp;c=E,1,6x_FqIN3L3lBg-wPwDn7aTxTNzIpA_cnOCtYltTA891hYy3jD_t0pgkRt3-H-OoGJ5tb5GRBNxrlb9SxV6LwYjsCR96x61B63YQbbPbmtoNsdtl8oW0,&amp;typo=1'>Internet Research: Ethical Guidelines 3.0</a> - https://aoir.org/ethics/ </li><li><a href='https://pervade.umd.edu/pervade-data-ethics-tool/'>PERVADE Data Ethics Tool</a> - https://pervade.umd.edu/pervade-data-ethics-tool/</li><li><a href='https://www.reddit.com/r/AskHistorians/comments/1iu4otk/meta_new_policy_for_researchers_using/'>AskHistorians Policy for Researchers using r/AskHistorians in Research</a> - https://www.reddit.com/r/AskHistorians/comments/1iu4otk/meta_new_policy_for_researchers_using/</li><li><a href='https://journals.sagepub.com/doi/full/10.1177/20539517211040759'>Excavating awareness and power in data science: A manifesto for trustworthy pervasive data research</a> - https://journals.sagepub.com/doi/full/10.1177/20539517211040759</li><li><a href='https://arxiv.org/pdf/2503.13752'>Beyond the Individual: A Community-Engaged Framework for Ethical Online Community Research</a> - https://arxiv.org/pdf/2503.13752</li></ul><p>Tool for large-scale disclosure: </p><ul><li><a href='https://journals.sagepub.com/doi/10.1177/20563051221077021'>Procedural and Substantive Ethics in the Design of Research Ethics Systems</a> - https://journals.sagepub.com/doi/10.1177/20563051221077021</li></ul><p> </p>]]></content:encoded>
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    <pubDate>Tue, 27 May 2025 11:00:00 -0400</pubDate>
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  <psc:chapter start="0:00" title="Engaging with Online Communities: Ethical Considerations for Researchers - On Research Podcast" />
  <psc:chapter start="0:30" title="Podcast Overview " />
  <psc:chapter start="2:27" title="Dr. Sarah Gilbert’s Background" />
  <psc:chapter start="5:17" title="Recap of the CMV Situation" />
  <psc:chapter start="6:27" title="Ethical Responsibilities in Research" />
  <psc:chapter start="8:44" title="Informed Consent Challenges" />
  <psc:chapter start="10:19" title="Disclosure in Deceptive Studies " />
  <psc:chapter start="11:37" title="Ethical Justifications for Concealing Identity" />
  <psc:chapter start="14:07" title="Impact on Community Trust" />
  <psc:chapter start="16:31" title="Balancing Rigor and Impact" />
  <psc:chapter start="20:50" title="Disclosure After Research" />
  <psc:chapter start="21:35" title="Understanding Community Nuance" />
  <psc:chapter start="25:51" title="Platform’s Role in Research Protections" />
  <psc:chapter start="29:53" title="IRB Limitations in Online Research" />
  <psc:chapter start="33:27" title="Resources for Ethical Research" />
  <psc:chapter start="36:44" title="Final Thoughts on Research Ethics" />
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    <itunes:duration>2288</itunes:duration>
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    <itunes:season>3</itunes:season>
    <itunes:episode>5</itunes:episode>
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    <itunes:title>CITI Program Turns 25: A Celebration of Commitment to Research Integrity - On Research Podcast</itunes:title>
    <title>CITI Program Turns 25: A Celebration of Commitment to Research Integrity - On Research Podcast</title>
    <itunes:summary><![CDATA[Today’s episode is a celebration of CITI Program’s 25th anniversary. We talk with a panel of long-time employees, including Jaime Arango, Vice President of Content and Education, Daniel Smith, Director of Content and Education, and Adiper Bello, Director of Operations and Support, about the history of CITI Program, key milestones in the company, and where CITI Program is headed.      Additional resources:  CITI Program timeline:  https://about.citiprogram.org/get-to-know-c...]]></itunes:summary>
    <description><![CDATA[<p>Today’s episode is a celebration of CITI Program’s 25th anniversary. We talk with a panel of long-time employees, including Jaime Arango, Vice President of Content and Education, Daniel Smith, Director of Content and Education, and Adiper Bello, Director of Operations and Support, about the history of CITI Program, key milestones in the company, and where CITI Program is headed.   <br/><br/></p><p>Additional resources: </p><ul><li>CITI Program timeline:  <a href='https://about.citiprogram.org/get-to-know-citi-program/'>https://about.citiprogram.org/get-to-know-citi-program/</a> </li></ul>]]></description>
    <content:encoded><![CDATA[<p>Today’s episode is a celebration of CITI Program’s 25th anniversary. We talk with a panel of long-time employees, including Jaime Arango, Vice President of Content and Education, Daniel Smith, Director of Content and Education, and Adiper Bello, Director of Operations and Support, about the history of CITI Program, key milestones in the company, and where CITI Program is headed.   <br/><br/></p><p>Additional resources: </p><ul><li>CITI Program timeline:  <a href='https://about.citiprogram.org/get-to-know-citi-program/'>https://about.citiprogram.org/get-to-know-citi-program/</a> </li></ul>]]></content:encoded>
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    <pubDate>Tue, 29 Apr 2025 09:00:00 -0400</pubDate>
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  <psc:chapter start="0:00" title="CITI Program Turns 25: A Celebration of Commitment to Research Integrity - On Research Podcast" />
  <psc:chapter start="0:05" title="Introduction Quote" />
  <psc:chapter start="0:51" title="New Host Introduction" />
  <psc:chapter start="2:42" title="25th Anniversary Celebration" />
  <psc:chapter start="3:40" title="Panelist Introductions" />
  <psc:chapter start="6:03" title="CITI Program’s Origin" />
  <psc:chapter start="6:25" title="Clarifying CITI’s Name" />
  <psc:chapter start="7:27" title="Evolution of CITI’s Mission" />
  <psc:chapter start="8:50" title="Pivotal Moments in History" />
  <psc:chapter start="11:18" title="Founding Context" />
  <psc:chapter start="13:25" title="Changes in Research Compliance" />
  <psc:chapter start="15:11" title="Memories from Long-Time Employees" />
  <psc:chapter start="18:39" title="Innovations and Initiatives " />
  <psc:chapter start="20:19" title="Response to COVID-19" />
  <psc:chapter start="21:40" title="Utilization of CITI Program" />
  <psc:chapter start="23:41" title="Company Culture" />
  <psc:chapter start="26:11" title="The Collaborative Nature of CITI Program" />
  <psc:chapter start="26:52" title="Challenges Ahead for Research Compliance" />
  <psc:chapter start="28:28" title="CITI Program’s Future Preparation" />
  <psc:chapter start="29:36" title="Subject Matter Experts and Collaboration" />
  <psc:chapter start="30:40" title="Message to Founders" />
  <psc:chapter start="32:10" title="Personal Reflections on 25 Years" />
  <psc:chapter start="35:25" title="Conclusion of the 25th Anniversary Episode" />
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    <itunes:duration>2197</itunes:duration>
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    <itunes:title>Community Engagement in Research - On Research Podcast</itunes:title>
    <title>Community Engagement in Research - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for a fascinating discussion with Dr. Jeremy Rossman, a researcher of 25 years, virologist, and President of a non-profit aimed at creating lasting and sustainable community development in research worldwide. We take a deep dive into community engagement in research; what it means, the challenges and opportunities, and why it’s so important. Jeremy does a wonderful job of explaining community engagement from all sides, whether you’re the researcher, the community involved in the resea...]]></itunes:summary>
    <description><![CDATA[<p>Join us for a fascinating discussion with Dr. Jeremy Rossman, a researcher of 25 years, virologist, and President of a non-profit aimed at creating lasting and sustainable community development in research worldwide. We take a deep dive into community engagement in research; what it means, the challenges and opportunities, and why it’s so important. Jeremy does a wonderful job of explaining community engagement from all sides, whether you’re the researcher, the community involved in the research, or the funding agency; it really takes all parties involved to work collaboratively towards improving research. <br/><br/>A special thank you to Cynthia Bellas for helping produce this episode! <br/><br/>Guest Bio: Dr. Jeremy Rossman is a virologist, President of the non-profit organization Research-Aid Networks, and an Honorary Senior Lecturer in Virology at the University of Kent. Dr. Rossman has conducted collaborative interdisciplinary research on the molecular biology of pandemic-causing viruses, international epidemic responses, evidence-based humanitarian aid and science education. Research-aid networks facilitate collaborative and evidence-based approaches for assessing need, delivering aid, evaluating effectiveness, and achieving equitable, long-term, sustainable community development worldwide. <br/><br/> <br/>Additional Resources: </p><ul><li>Dr. Rossman’s Non-Profit Research-Aid Networks - <a href='https://researchaidnetworks.org/'>https://researchaidnetworks.org/</a></li><li>NIH Community Engagement Alliance - <a href='https://ceal.nih.gov/'>https://ceal.nih.gov/</a></li><li>Long-COVID Patient-Led Research Collaborative - <a href='https://patientresearchcovid19.com/'>https://patientresearchcovid19.com/</a></li><li>Learn more about HRP Consulting here - <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul>]]></description>
    <content:encoded><![CDATA[<p>Join us for a fascinating discussion with Dr. Jeremy Rossman, a researcher of 25 years, virologist, and President of a non-profit aimed at creating lasting and sustainable community development in research worldwide. We take a deep dive into community engagement in research; what it means, the challenges and opportunities, and why it’s so important. Jeremy does a wonderful job of explaining community engagement from all sides, whether you’re the researcher, the community involved in the research, or the funding agency; it really takes all parties involved to work collaboratively towards improving research. <br/><br/>A special thank you to Cynthia Bellas for helping produce this episode! <br/><br/>Guest Bio: Dr. Jeremy Rossman is a virologist, President of the non-profit organization Research-Aid Networks, and an Honorary Senior Lecturer in Virology at the University of Kent. Dr. Rossman has conducted collaborative interdisciplinary research on the molecular biology of pandemic-causing viruses, international epidemic responses, evidence-based humanitarian aid and science education. Research-aid networks facilitate collaborative and evidence-based approaches for assessing need, delivering aid, evaluating effectiveness, and achieving equitable, long-term, sustainable community development worldwide. <br/><br/> <br/>Additional Resources: </p><ul><li>Dr. Rossman’s Non-Profit Research-Aid Networks - <a href='https://researchaidnetworks.org/'>https://researchaidnetworks.org/</a></li><li>NIH Community Engagement Alliance - <a href='https://ceal.nih.gov/'>https://ceal.nih.gov/</a></li><li>Long-COVID Patient-Led Research Collaborative - <a href='https://patientresearchcovid19.com/'>https://patientresearchcovid19.com/</a></li><li>Learn more about HRP Consulting here - <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul>]]></content:encoded>
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    <pubDate>Tue, 25 Mar 2025 11:00:00 -0400</pubDate>
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  <item>
    <itunes:title>Dual Use Research of Concern Policy - On Research Podcast</itunes:title>
    <title>Dual Use Research of Concern Policy - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for a fascinating discussion about the recently updated Dual Use Research of Concern policy. There was so much to cover that I brought in two experts – one as my co-host and the other as our guest. If you don’t know much about Dual Use Research of Concern, this conversation will be a fantastic primer. We discuss what Dual Use means, the policy updates, how these updates could impact your research institution, and why all of this matters.   Also of note, we recorded this episode a...]]></itunes:summary>
    <description><![CDATA[<p>Join us for a fascinating discussion about the recently updated Dual Use Research of Concern policy. There was so much to cover that I brought in two experts – one as my co-host and the other as our guest. If you don’t know much about Dual Use Research of Concern, this conversation will be a fantastic primer. We discuss what Dual Use means, the policy updates, how these updates could impact your research institution, and why all of this matters.  </p><p>Also of note, we recorded this episode a couple of weeks ago, in the midst of the many executive orders impacting research. Anne and Melissa do share their thoughts on how you should move forward in this gray area we’ve all found ourselves in, but we always encourage folks to stay up to date as much as possible on the evolving landscape.      </p><p> </p><p>Additional Resources: </p><ul><li>DURC Policy released May 2024, effective May 2025 - <a href='https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-Policy-for-Oversight-of-DURC-and-PEPP.pdf'>https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-Policy-for-Oversight-of-DURC-and-PEPP.pdf</a></li><li>Implementation Guidance for DURC policy - <a href='https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-DURC-PEPP-Implementation-Guidance.pdf'>https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-DURC-PEPP-Implementation-Guidance.pdf</a></li><li>Learn more about HRP Consulting: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/></p><p>Guest Bios: </p><p>Melissa James – Guest – Melissa is the BSL-3 Facility Manager for Yale University with 12+ years of high containment experience, including establishing and maintaining compliance with the Federal Select Agent Program. Her degrees in biology and Homeland Security and RBP credentials position her to share her vast knowledge and experience with others in the field.</p><p>Anne Hawkinsbadge – Guest Host – Anne is the Assistant Director of EHS. She is a Certified Safety Professional, Certified Healthcare Safety Professional, Certified Healthcare Emergency Professional, and a Chemist with the American Society of Clinical Pathology. Her work experience includes healthcare, auto manufacturing, pharmaceutical, academia, worker compensation insurance, and chemical manufacturing. </p>]]></description>
    <content:encoded><![CDATA[<p>Join us for a fascinating discussion about the recently updated Dual Use Research of Concern policy. There was so much to cover that I brought in two experts – one as my co-host and the other as our guest. If you don’t know much about Dual Use Research of Concern, this conversation will be a fantastic primer. We discuss what Dual Use means, the policy updates, how these updates could impact your research institution, and why all of this matters.  </p><p>Also of note, we recorded this episode a couple of weeks ago, in the midst of the many executive orders impacting research. Anne and Melissa do share their thoughts on how you should move forward in this gray area we’ve all found ourselves in, but we always encourage folks to stay up to date as much as possible on the evolving landscape.      </p><p> </p><p>Additional Resources: </p><ul><li>DURC Policy released May 2024, effective May 2025 - <a href='https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-Policy-for-Oversight-of-DURC-and-PEPP.pdf'>https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-Policy-for-Oversight-of-DURC-and-PEPP.pdf</a></li><li>Implementation Guidance for DURC policy - <a href='https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-DURC-PEPP-Implementation-Guidance.pdf'>https://bidenwhitehouse.archives.gov/wp-content/uploads/2024/05/USG-DURC-PEPP-Implementation-Guidance.pdf</a></li><li>Learn more about HRP Consulting: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/></p><p>Guest Bios: </p><p>Melissa James – Guest – Melissa is the BSL-3 Facility Manager for Yale University with 12+ years of high containment experience, including establishing and maintaining compliance with the Federal Select Agent Program. Her degrees in biology and Homeland Security and RBP credentials position her to share her vast knowledge and experience with others in the field.</p><p>Anne Hawkinsbadge – Guest Host – Anne is the Assistant Director of EHS. She is a Certified Safety Professional, Certified Healthcare Safety Professional, Certified Healthcare Emergency Professional, and a Chemist with the American Society of Clinical Pathology. Her work experience includes healthcare, auto manufacturing, pharmaceutical, academia, worker compensation insurance, and chemical manufacturing. </p>]]></content:encoded>
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    <pubDate>Tue, 25 Feb 2025 10:00:00 -0500</pubDate>
    <itunes:duration>2463</itunes:duration>
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    <itunes:episode>2</itunes:episode>
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  <item>
    <itunes:title>Coverage Analysis in Clinical Research - On Research Podcast</itunes:title>
    <title>Coverage Analysis in Clinical Research - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for episode 1 of season 3 as we explore an essential compliance topic: coverage analysis. It’s a complicated process, but lucky for us, we have Andra Popa. Andra is an expert with nearly two decades of experience in healthcare law, compliance, and coverage analysis. As one of the first in the industry to provide coverage analysis, Andra walks us through the intricate details of the process, including why it’s so important and the consequences if you don’t have a proper coverage analys...]]></itunes:summary>
    <description><![CDATA[<p>Join us for episode 1 of season 3 as we explore an essential compliance topic: coverage analysis. It’s a complicated process, but lucky for us, we have Andra Popa. Andra is an expert with nearly two decades of experience in healthcare law, compliance, and coverage analysis. As one of the first in the industry to provide coverage analysis, Andra walks us through the intricate details of the process, including why it’s so important and the consequences if you don’t have a proper coverage analysis process in place.     <br/> </p><p>Additional Resources: </p><ul><li>Local Coverage Determinations CMS - <a href='https://www.cms.gov/medicare/coverage/determination-process/local'>https://www.cms.gov/medicare/coverage/determination-process/local</a></li><li>National Coverage Determinations CMS - <a href='https://www.cms.gov/medicare-coverage-database/search-results.aspx?keyword=nat&amp;areaId=all&amp;docType=NCD'>https://www.cms.gov/medicare-coverage-database/search-results.aspx?keyword=nat&amp;areaId=all&amp;docType=NCD</a></li><li><em>Thorny Medicare Coverage Issues</em> article by Andra Popa - <a href='https://compliancecosmos.org/thorny-medicare-coverage-issues'>https://compliancecosmos.org/thorny-medicare-coverage-issues</a></li><li>Learn more about HRP Consulting here: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Andra Popa is responsible for healthcare content at CITI Programs and was part of the first group to conduct Medicare Coverage Analyses. She owned a consulting firm that worked with over 40 healthcare entities to create, assess, audit, and monitor compliance programs, as well as to create educational programs. A graduate of Boston College with degrees in English and economics, she also has JD and LLM (healthcare law) degrees from Loyola University Chicago School of Law. She has published over 100 articles, written book chapters, and conducted workshops in design and compliance.</p><p> </p><p> </p>]]></description>
    <content:encoded><![CDATA[<p>Join us for episode 1 of season 3 as we explore an essential compliance topic: coverage analysis. It’s a complicated process, but lucky for us, we have Andra Popa. Andra is an expert with nearly two decades of experience in healthcare law, compliance, and coverage analysis. As one of the first in the industry to provide coverage analysis, Andra walks us through the intricate details of the process, including why it’s so important and the consequences if you don’t have a proper coverage analysis process in place.     <br/> </p><p>Additional Resources: </p><ul><li>Local Coverage Determinations CMS - <a href='https://www.cms.gov/medicare/coverage/determination-process/local'>https://www.cms.gov/medicare/coverage/determination-process/local</a></li><li>National Coverage Determinations CMS - <a href='https://www.cms.gov/medicare-coverage-database/search-results.aspx?keyword=nat&amp;areaId=all&amp;docType=NCD'>https://www.cms.gov/medicare-coverage-database/search-results.aspx?keyword=nat&amp;areaId=all&amp;docType=NCD</a></li><li><em>Thorny Medicare Coverage Issues</em> article by Andra Popa - <a href='https://compliancecosmos.org/thorny-medicare-coverage-issues'>https://compliancecosmos.org/thorny-medicare-coverage-issues</a></li><li>Learn more about HRP Consulting here: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Andra Popa is responsible for healthcare content at CITI Programs and was part of the first group to conduct Medicare Coverage Analyses. She owned a consulting firm that worked with over 40 healthcare entities to create, assess, audit, and monitor compliance programs, as well as to create educational programs. A graduate of Boston College with degrees in English and economics, she also has JD and LLM (healthcare law) degrees from Loyola University Chicago School of Law. She has published over 100 articles, written book chapters, and conducted workshops in design and compliance.</p><p> </p><p> </p>]]></content:encoded>
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    <pubDate>Tue, 28 Jan 2025 11:00:00 -0500</pubDate>
    <itunes:duration>3064</itunes:duration>
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    <itunes:title>PRIM&amp;R 2024 Conference Recap - On Research Podcast</itunes:title>
    <title>PRIM&amp;R 2024 Conference Recap - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for an engaging recap of the recent PRIM&amp;R conference, held on November 17-20 in Seattle. With an amazing panel of research professionals, we discuss the highlights, popular sessions, hot topics, and the benefits of attending this conference. Whether you attended or not, there is plenty of valuable information shared by the panel of experts in our field.      Guest panel for this episode: Jaime Arango, Vice President of Content and Education at CITI Program; Rafaell...]]></itunes:summary>
    <description><![CDATA[<p>Join us for an engaging recap of the recent PRIM&amp;R conference, held on November 17-20 in Seattle. With an amazing panel of research professionals, we discuss the highlights, popular sessions, hot topics, and the benefits of attending this conference. Whether you attended or not, there is plenty of valuable information shared by the panel of experts in our field.    <br/><br/>Guest panel for this episode: Jaime Arango, Vice President of Content and Education at CITI Program; Rafaella Hart, Senior Vice President of IRB, IBC &amp; QA at BRANY; Karen Christianson, Senior Vice President and Managing Director of the HRP Consulting Group; Walden Leverich, Senior Vice President and Managing Director of Tech Software; and Nate Ferguson, a consultant and IRB Analyst who collaborates with a variety of clients, including footwear and apparel companies conducting human subjects research.<br/><br/><br/>Additional Resources: </p><ul><li>PRIM&amp;R’s 50th-anniversary blog post - <a href='https://blog.primr.org/the-history-of-primrs-conferences/'>https://blog.primr.org/the-history-of-primrs-conferences/</a></li><li>Learn more about HRP Consulting here - <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul>]]></description>
    <content:encoded><![CDATA[<p>Join us for an engaging recap of the recent PRIM&amp;R conference, held on November 17-20 in Seattle. With an amazing panel of research professionals, we discuss the highlights, popular sessions, hot topics, and the benefits of attending this conference. Whether you attended or not, there is plenty of valuable information shared by the panel of experts in our field.    <br/><br/>Guest panel for this episode: Jaime Arango, Vice President of Content and Education at CITI Program; Rafaella Hart, Senior Vice President of IRB, IBC &amp; QA at BRANY; Karen Christianson, Senior Vice President and Managing Director of the HRP Consulting Group; Walden Leverich, Senior Vice President and Managing Director of Tech Software; and Nate Ferguson, a consultant and IRB Analyst who collaborates with a variety of clients, including footwear and apparel companies conducting human subjects research.<br/><br/><br/>Additional Resources: </p><ul><li>PRIM&amp;R’s 50th-anniversary blog post - <a href='https://blog.primr.org/the-history-of-primrs-conferences/'>https://blog.primr.org/the-history-of-primrs-conferences/</a></li><li>Learn more about HRP Consulting here - <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul>]]></content:encoded>
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    <pubDate>Thu, 12 Dec 2024 09:00:00 -0500</pubDate>
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  <psc:chapter start="2:29" title="Initial Impressions of PRIM&amp;R" />
  <psc:chapter start="4:25" title="Reflections on Conference Topics " />
  <psc:chapter start="5:29" title="The Importance of In-Person Connections " />
  <psc:chapter start="6:43" title="First-Time Attendee Experience " />
  <psc:chapter start="7:15" title="Common Challenges Discussed " />
  <psc:chapter start="8:18" title="Shift in AI Discussions " />
  <psc:chapter start="9:23" title="AI as a Tool in Research " />
  <psc:chapter start="10:47" title="Single IRB Mandate Conversations" />
  <psc:chapter start="12:07" title="Navigating the Single IRB Landscape " />
  <psc:chapter start="14:24" title="Combining Conferences: A New Approach " />
  <psc:chapter start="16:16" title="Challenges of Budget Constraints " />
  <psc:chapter start="17:00" title="Takeaways for Non-Attendees " />
  <psc:chapter start="18:16" title="Regulatory Agency Interactions " />
  <psc:chapter start="19:04" title="Local Conferences as Alternatives " />
  <psc:chapter start="20:06" title="Quality of Content Justifies Attendance " />
  <psc:chapter start="21:11" title="The Importance of Attending Conferences " />
  <psc:chapter start="22:47" title="Sharing Knowledge in the Industry " />
  <psc:chapter start="23:52" title="Documenting Institutional Knowledge " />
  <psc:chapter start="24:25" title="How to Present at Conferences " />
  <psc:chapter start="27:20" title="Overcoming First-Time Speaker Anxiety " />
  <psc:chapter start="28:46" title="Flexibility in Presentation Topics " />
  <psc:chapter start="30:16" title="Engaging Presentation Topics " />
  <psc:chapter start="30:55" title="Submission Timeline for Conference Proposals " />
  <psc:chapter start="31:59" title="Volunteering for Conference Committees " />
  <psc:chapter start="33:10" title="Collaborative Session Ideas " />
  <psc:chapter start="34:28" title="Audience Engagement in Presentations " />
  <psc:chapter start="35:32" title="Discussion on Political Changes Impacting Research " />
  <psc:chapter start="36:35" title="Local Context in Research Regulations " />
  <psc:chapter start="40:18" title="Navigating Changes in Research Responsibilities " />
  <psc:chapter start="40:49" title="Self-Regulation in Non-Covered Entities " />
  <psc:chapter start="41:31" title="Vendor Perspectives in the Exhibit Hall " />
  <psc:chapter start="43:17" title="Conference Atmosphere " />
  <psc:chapter start="44:13" title="Exhibitor Engagement Strategies " />
  <psc:chapter start="45:19" title="Exhibitor Theater Concept " />
  <psc:chapter start="45:41" title="Conference Size Comparison " />
  <psc:chapter start="47:28" title="Physical Space Impact " />
  <psc:chapter start="48:37" title="Lunch Logistics Discussion " />
  <psc:chapter start="52:46" title="Final Thoughts on Conference Value " />
  <psc:chapter start="55:34" title="Encouragement to Explore Diverse Sessions " />
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    <itunes:title>Updated Research Misconduct Final Rule - On Research Podcast</itunes:title>
    <title>Updated Research Misconduct Final Rule - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for an in-depth discussion about the updated research misconduct final rule.  John Baughman, a research compliance expert, gives an excellent overview of the updates, why they matter, and how to be prepared when the policy goes into effect on January 1, 2025. While we all wait for the templates and guidance documents from the Office of Research Integrity, John provides some excellent advice and breaks down the most important elements of the new final rule.   Additional Resou...]]></itunes:summary>
    <description><![CDATA[<p>Join us for an in-depth discussion about the updated research misconduct final rule.  John Baughman, a research compliance expert, gives an excellent overview of the updates, why they matter, and how to be prepared when the policy goes into effect on January 1, 2025. While we all wait for the templates and guidance documents from the Office of Research Integrity, John provides some excellent advice and breaks down the most important elements of the new final rule.  </p><p>Additional Resources: </p><ul><li>The Updated Final Rule on Research Misconduct - <a href='https://www.federalregister.gov/documents/2024/09/17/2024-20814/public-health-service-policies-on-research-misconduct'>https://www.federalregister.gov/documents/2024/09/17/2024-20814/public-health-service-policies-on-research-misconduct</a></li><li>Blog from ORI about the updated final rule - <a href='https://ori.hhs.gov/blog/ori-final-rule'>https://ori.hhs.gov/blog/ori-final-rule</a></li><li>Learn more about HRP Consulting - <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: John R. Baumann, Ph.D., was the Associate Vice President for Research Compliance at Indiana University, including the Bloomington and Indianapolis campuses, as well as the five regional campuses and affiliated hospitals. Dr. Baumann has over 25 years of experience in research, research administration, responsible conduct of research, and research compliance. He has had direct-line responsibility for all aspects of research compliance with regulations and ethical standards related to research misconduct, human subjects research, research with animals, conflict of interest, radiation, and biological safety, as well as research development, coordination, and submission of grant and contract applications, and management of funded research.  </p>]]></description>
    <content:encoded><![CDATA[<p>Join us for an in-depth discussion about the updated research misconduct final rule.  John Baughman, a research compliance expert, gives an excellent overview of the updates, why they matter, and how to be prepared when the policy goes into effect on January 1, 2025. While we all wait for the templates and guidance documents from the Office of Research Integrity, John provides some excellent advice and breaks down the most important elements of the new final rule.  </p><p>Additional Resources: </p><ul><li>The Updated Final Rule on Research Misconduct - <a href='https://www.federalregister.gov/documents/2024/09/17/2024-20814/public-health-service-policies-on-research-misconduct'>https://www.federalregister.gov/documents/2024/09/17/2024-20814/public-health-service-policies-on-research-misconduct</a></li><li>Blog from ORI about the updated final rule - <a href='https://ori.hhs.gov/blog/ori-final-rule'>https://ori.hhs.gov/blog/ori-final-rule</a></li><li>Learn more about HRP Consulting - <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: John R. Baumann, Ph.D., was the Associate Vice President for Research Compliance at Indiana University, including the Bloomington and Indianapolis campuses, as well as the five regional campuses and affiliated hospitals. Dr. Baumann has over 25 years of experience in research, research administration, responsible conduct of research, and research compliance. He has had direct-line responsibility for all aspects of research compliance with regulations and ethical standards related to research misconduct, human subjects research, research with animals, conflict of interest, radiation, and biological safety, as well as research development, coordination, and submission of grant and contract applications, and management of funded research.  </p>]]></content:encoded>
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    <pubDate>Tue, 10 Dec 2024 10:00:00 -0500</pubDate>
    <itunes:duration>2495</itunes:duration>
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    <itunes:episode>11</itunes:episode>
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  <item>
    <itunes:title>The Role of Pharmacy in Research - On Research Podcast</itunes:title>
    <title>The Role of Pharmacy in Research - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for a fascinating discussion about the evolution of pharmacy in clinical research. Adam Samson, Head of Clinical Delivery Operations at Walgreens, discusses how pharmacists and pharmacy techs have more opportunities to participate in clinical trials. Learn how Walgreens has developed its research program to include the pharmacy at the center of its operations. This program includes takeaways that any research organization can learn from, including how best to include pharmacists and t...]]></itunes:summary>
    <description><![CDATA[<p>Join us for a fascinating discussion about the evolution of pharmacy in clinical research. Adam Samson, Head of Clinical Delivery Operations at Walgreens, discusses how pharmacists and pharmacy techs have more opportunities to participate in clinical trials. Learn how Walgreens has developed its research program to include the pharmacy at the center of its operations. This program includes takeaways that any research organization can learn from, including how best to include pharmacists and techs in future research.  </p><p>Additional Resources: </p><ul><li>Learn more about clinical trials at Walgreens: <a href='https://go.walgreenshealth.com/clinicaltrials'>https://go.walgreenshealth.com/clinicaltrials</a></li><li>Article about the evolving role of pharmacists in research: <a href='https://pharmddegree.com/careers/research-pharmacist/'>https://pharmddegree.com/careers/research-pharmacist/</a></li><li>Learn more about HRP Consulting here: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p>Guest Bio: Adam Samson has 15 years of experience designing and executing clinical trials across multiple therapeutic areas, phases, and treatment modalities. Adam is a clinical research executive passionate about bringing clinical trials closer to patients through community pharmacies and other innovative models. Adam also serves as an Adjunct Faculty at George Washington University in the Regulatory Affairs and Clinical Research Leadership Graduate Program. He volunteers with several non-profit organizations that aim to improve the clinical research industry through pre-competitive collaborations.  </p>]]></description>
    <content:encoded><![CDATA[<p>Join us for a fascinating discussion about the evolution of pharmacy in clinical research. Adam Samson, Head of Clinical Delivery Operations at Walgreens, discusses how pharmacists and pharmacy techs have more opportunities to participate in clinical trials. Learn how Walgreens has developed its research program to include the pharmacy at the center of its operations. This program includes takeaways that any research organization can learn from, including how best to include pharmacists and techs in future research.  </p><p>Additional Resources: </p><ul><li>Learn more about clinical trials at Walgreens: <a href='https://go.walgreenshealth.com/clinicaltrials'>https://go.walgreenshealth.com/clinicaltrials</a></li><li>Article about the evolving role of pharmacists in research: <a href='https://pharmddegree.com/careers/research-pharmacist/'>https://pharmddegree.com/careers/research-pharmacist/</a></li><li>Learn more about HRP Consulting here: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p>Guest Bio: Adam Samson has 15 years of experience designing and executing clinical trials across multiple therapeutic areas, phases, and treatment modalities. Adam is a clinical research executive passionate about bringing clinical trials closer to patients through community pharmacies and other innovative models. Adam also serves as an Adjunct Faculty at George Washington University in the Regulatory Affairs and Clinical Research Leadership Graduate Program. He volunteers with several non-profit organizations that aim to improve the clinical research industry through pre-competitive collaborations.  </p>]]></content:encoded>
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    <pubDate>Tue, 29 Oct 2024 09:00:00 -0400</pubDate>
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  <psc:chapter start="0:00" title="The Role of Pharmacists in Clinical Trials " />
  <psc:chapter start="0:19" title="Introduction to the Episode " />
  <psc:chapter start="1:43" title="Adam Sampson&#39;s Background " />
  <psc:chapter start="3:22" title="Current Role of Pharmacists in Research " />
  <psc:chapter start="5:22" title="Pharmacists in Independent Research Sites " />
  <psc:chapter start="6:25" title="Benefits of Pharmacists in Research " />
  <psc:chapter start="7:39" title="Complex Trial Designs and Pharmacists " />
  <psc:chapter start="9:44" title="Decentralized Trials and Pharmacists" />
  <psc:chapter start="11:39" title="Patient Trust in Pharmacists " />
  <psc:chapter start="12:47" title="Integration of Pharmacy and Clinical Trials " />
  <psc:chapter start="14:48" title="Hurdles in Pharmacy-Based Research " />
  <psc:chapter start="16:03" title="Crawl, Walk, Run Approach " />
  <psc:chapter start="19:04" title="Education and Awareness in Research " />
  <psc:chapter start="20:10" title="Community Engagement Initiatives " />
  <psc:chapter start="21:57" title="Grassroots Education Efforts " />
  <psc:chapter start="23:31" title="Pharmacists as Trusted Information Sources " />
  <psc:chapter start="24:22" title="Study Design Involvement " />
  <psc:chapter start="26:16" title="Pharmacy Technicians&#39; Opportunities " />
  <psc:chapter start="27:22" title="Pharmacists&#39; Evolving Clinical Role " />
  <psc:chapter start="28:45" title="Microfilming Technology " />
  <psc:chapter start="29:53" title="Specialty Pharmacy Management " />
  <psc:chapter start="30:21" title="Translating MTM to Research " />
  <psc:chapter start="32:59" title="Building a Site Management Organization " />
  <psc:chapter start="35:21" title="Privacy and Patient Data Consent " />
  <psc:chapter start="36:07" title="Patient Recruitment Process " />
  <psc:chapter start="38:52" title="Opting In and Out of Research " />
  <psc:chapter start="41:01" title="Communication with Patients " />
  <psc:chapter start="42:20" title="Pharmacy Education Evolution " />
  <psc:chapter start="45:01" title="Same Team Segment " />
  <psc:chapter start="47:52" title="Closing statement " />
</psc:chapters>
    <itunes:duration>2897</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>10</itunes:episode>
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  <item>
    <itunes:title>Practical Uses of AI in Research - On Research Podcast</itunes:title>
    <title>Practical Uses of AI in Research - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for a deep dive into the world of AI and its practical applications in the world of research operations. Charlie Fremont, an EHR application analyst specializing in research operations and billing, discusses how AI technology has helped him create new workflows that have vastly improved processes. Not only does he share details around how he uses this technology, he also shares valuable insight into the limitations and potential risks of using these tools. We also discuss AI’s impact ...]]></itunes:summary>
    <description><![CDATA[<p>Join us for a deep dive into the world of AI and its practical applications in the world of research operations. Charlie Fremont, an EHR application analyst specializing in research operations and billing, discusses how AI technology has helped him create new workflows that have vastly improved processes. Not only does he share details around how he uses this technology, he also shares valuable insight into the limitations and potential risks of using these tools. We also discuss AI’s impact on productivity in general and sorting through the proper balance of efficiencies with compliance.    </p><p><br/></p><p>Additional Resources: </p><ul><li>The AI Risk Repository: A Comprehensive Meta-Review, Database and Taxonomy of Risks from AI - <a href='https://arxiv.org/abs/2408.12622'>https://arxiv.org/abs/2408.12622</a></li><li>Deloitte Report – How Generative AI can reshape the health frontier - <a href='https://www2.deloitte.com/content/dam/Deloitte/us/Documents/life-sciences-health-care/us-from-code-to-cure-1.pdf'>https://www2.deloitte.com/content/dam/Deloitte/us/Documents/life-sciences-health-care/us-from-code-to-cure-1.pdf</a></li><li>Learn more about HRP Consulting: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Charlie Fremont is an Epic EHR Application Analyst and independent consultant with extensive research and billing experience. With 15 years in the healthcare industry and 10 years in research, Charlie specializes in leveraging technologies such as ChatGPT, Python, and Excel Formulas/VBA. Charles has successfully implemented solutions that streamline workflows and improve operational efficiency, which he shares openly with colleagues in our research industry.  </p>]]></description>
    <content:encoded><![CDATA[<p>Join us for a deep dive into the world of AI and its practical applications in the world of research operations. Charlie Fremont, an EHR application analyst specializing in research operations and billing, discusses how AI technology has helped him create new workflows that have vastly improved processes. Not only does he share details around how he uses this technology, he also shares valuable insight into the limitations and potential risks of using these tools. We also discuss AI’s impact on productivity in general and sorting through the proper balance of efficiencies with compliance.    </p><p><br/></p><p>Additional Resources: </p><ul><li>The AI Risk Repository: A Comprehensive Meta-Review, Database and Taxonomy of Risks from AI - <a href='https://arxiv.org/abs/2408.12622'>https://arxiv.org/abs/2408.12622</a></li><li>Deloitte Report – How Generative AI can reshape the health frontier - <a href='https://www2.deloitte.com/content/dam/Deloitte/us/Documents/life-sciences-health-care/us-from-code-to-cure-1.pdf'>https://www2.deloitte.com/content/dam/Deloitte/us/Documents/life-sciences-health-care/us-from-code-to-cure-1.pdf</a></li><li>Learn more about HRP Consulting: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Charlie Fremont is an Epic EHR Application Analyst and independent consultant with extensive research and billing experience. With 15 years in the healthcare industry and 10 years in research, Charlie specializes in leveraging technologies such as ChatGPT, Python, and Excel Formulas/VBA. Charles has successfully implemented solutions that streamline workflows and improve operational efficiency, which he shares openly with colleagues in our research industry.  </p>]]></content:encoded>
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    <pubDate>Tue, 24 Sep 2024 11:00:00 -0400</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Practical Uses of AI in Research - On Research Podcast" />
  <psc:chapter start="0:26" title="Podcast Introduction" />
  <psc:chapter start="2:20" title="Charlie&#39;s Journey into Research" />
  <psc:chapter start="4:14" title="Defining AI Terms " />
  <psc:chapter start="6:09" title="Generative AI vs. Predictive AI" />
  <psc:chapter start="7:20" title="AI Adoption in Research " />
  <psc:chapter start="8:35" title="Real-Life Applications of Generative AI" />
  <psc:chapter start="9:30" title="Generative AI in Research Building " />
  <psc:chapter start="9:57" title="Challenges of AI Adoption" />
  <psc:chapter start="10:19" title="Using Generative AI for Coding " />
  <psc:chapter start="12:40" title="Bridging IT and Research" />
  <psc:chapter start="14:01" title="Everyday Applications of AI " />
  <psc:chapter start="16:02" title="Understanding ChatGPT" />
  <psc:chapter start="16:30" title="Verifying Information from AI " />
  <psc:chapter start="19:08" title="Caution with AI Use" />
  <psc:chapter start="20:04" title="AI’s Cultural Integration" />
  <psc:chapter start="21:08" title="Limitations of AI in Research" />
  <psc:chapter start="21:31" title="The Importance of AI Adoption " />
  <psc:chapter start="22:27" title="Risks of Using Generative AI " />
  <psc:chapter start="23:09" title="Data Confidentiality in AI Tools " />
  <psc:chapter start="24:28" title="Institutional Policy and Compliance" />
  <psc:chapter start="25:56" title="Using AI for Secure Data Handling " />
  <psc:chapter start="28:26" title="Generative AI and Cognitive Dependency " />
  <psc:chapter start="30:26" title="Shifting Roles with AI Integration " />
  <psc:chapter start="32:04" title="Collaboration Between Experts and AI " />
  <psc:chapter start="35:12" title="Finding Balance in AI Capabilities " />
  <psc:chapter start="38:23" title="Deep Work vs. Shallow Work" />
  <psc:chapter start="40:25" title="Preventing Burnout with AI Tools" />
  <psc:chapter start="41:22" title="The Challenges of Clinical Research" />
  <psc:chapter start="42:05" title="AI&#39;s Role in Reducing Workload" />
  <psc:chapter start="43:58" title="Real-Life Applications of AI " />
  <psc:chapter start="44:40" title="Same Team Segment: Connecting with Purpose in Research " />
  <psc:chapter start="46:53" title="Closing Remarks and Podcast Promotion " />
</psc:chapters>
    <itunes:duration>2838</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>9</itunes:episode>
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  <item>
    <itunes:title>Politics and Research: Transferrable Skills - On Research Podcast</itunes:title>
    <title>Politics and Research: Transferrable Skills - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for a fascinating discussion about the intersection of Research and Politics. Rachel Baker, a research nurse and House Representative in the state of Ohio, discusses working in two very different fields and how they both inform each other. We focus on the similarities of the fields and the transferable skills that Rachel has learned from her political career that have helped in her research role.     Additional Resources:  Ohio House of Representatives website - https:/...]]></itunes:summary>
    <description><![CDATA[<p>Join us for a fascinating discussion about the intersection of Research and Politics. Rachel Baker, a research nurse and House Representative in the state of Ohio, discusses working in two very different fields and how they both inform each other. We focus on the similarities of the fields and the transferable skills that Rachel has learned from her political career that have helped in her research role.  </p><p> </p><p>Additional Resources: </p><ul><li>Ohio House of Representatives website - <a href='https://ohiohouse.gov/members/rachel-b-baker'>https://ohiohouse.gov/members/rachel-b-baker</a></li><li>Learn more about <a href='https://thehrpconsultinggroup.com/'>HRP Consulting</a>: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Rachel Baker has earned a BSN, MSW, and PhD. She works as a Nurse Researcher and teaches Research and Biostatistics to graduate nursing students. She also serves as the State Representative for Ohio’s HD27. In her first year, she sponsored 13 bills addressing topics including adoption modernization, access to MAT for opioid use disorder, Adverse Childhood Experiences, healthcare workplace violence, &amp; childhood exposure to lead. She serves on the Aviation &amp; Aerospace Committee, Behavioral Health Committee, Health Provider Services Committee, Public Health Policy Committee, and Technology &amp; Innovation Committee. She was appointed to the OneOhio Recovery Foundation Board and the Ohio Children’s Trust Fund Board. </p>]]></description>
    <content:encoded><![CDATA[<p>Join us for a fascinating discussion about the intersection of Research and Politics. Rachel Baker, a research nurse and House Representative in the state of Ohio, discusses working in two very different fields and how they both inform each other. We focus on the similarities of the fields and the transferable skills that Rachel has learned from her political career that have helped in her research role.  </p><p> </p><p>Additional Resources: </p><ul><li>Ohio House of Representatives website - <a href='https://ohiohouse.gov/members/rachel-b-baker'>https://ohiohouse.gov/members/rachel-b-baker</a></li><li>Learn more about <a href='https://thehrpconsultinggroup.com/'>HRP Consulting</a>: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Rachel Baker has earned a BSN, MSW, and PhD. She works as a Nurse Researcher and teaches Research and Biostatistics to graduate nursing students. She also serves as the State Representative for Ohio’s HD27. In her first year, she sponsored 13 bills addressing topics including adoption modernization, access to MAT for opioid use disorder, Adverse Childhood Experiences, healthcare workplace violence, &amp; childhood exposure to lead. She serves on the Aviation &amp; Aerospace Committee, Behavioral Health Committee, Health Provider Services Committee, Public Health Policy Committee, and Technology &amp; Innovation Committee. She was appointed to the OneOhio Recovery Foundation Board and the Ohio Children’s Trust Fund Board. </p>]]></content:encoded>
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    <pubDate>Tue, 27 Aug 2024 10:00:00 -0400</pubDate>
    <itunes:duration>2621</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>8</itunes:episode>
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  <item>
    <itunes:title>Quality Improvement vs. Research: What&#39;s the Difference? - On Research Podcast</itunes:title>
    <title>Quality Improvement vs. Research: What&#39;s the Difference? - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for a discussion about the always-interesting topic of Quality Improvement vs. Research. What is the difference between QI and Research, and how do researchers and IRBs determine the difference between the two? Tiffany Gommel shares her experience, some helpful insights, and practical advice on this topic.     Additional Resources:  Example of QI vs Research Checklist from NIH - https://irbo.nih.gov/confluence/download/attachments/70321066/QA-QI%20vs.%20Research.pdf?version=...]]></itunes:summary>
    <description><![CDATA[<p>Join us for a discussion about the always-interesting topic of Quality Improvement vs. Research. What is the difference between QI and Research, and how do researchers and IRBs determine the difference between the two? Tiffany Gommel shares her experience, some helpful insights, and practical advice on this topic.  <br/><br/></p><p>Additional Resources: </p><ul><li>Example of QI vs Research Checklist from NIH - <a href='https://irbo.nih.gov/confluence/download/attachments/70321066/QA-QI%20vs.%20Research.pdf?version=1&amp;modificationDate=1645630780163&amp;api=v2'>https://irbo.nih.gov/confluence/download/attachments/70321066/QA-QI%20vs.%20Research.pdf?version=1&amp;modificationDate=1645630780163&amp;api=v2</a></li><li>Example guidance of QI vs Research from Icahn School of Medicine - <a href='https://researchroadmap.mssm.edu/other-research/cnri/ebp-qi-research/'>https://researchroadmap.mssm.edu/other-research/cnri/ebp-qi-research/</a></li><li>Learn more about HRP Consulting here - <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Tiffany Gommel, the Director of the Office of IRB Operations (IRBO) at the National Institutes of Health (NIH) for the Intramural Research Program, is responsible for the operation and support of the NIH IRB, which reviews and approves human subjects research from the 27 Institutes across the NIH. With over two decades of clinical research experience, Tiffany has valuable expertise running IRBs at multiple organizations.<br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p>Join us for a discussion about the always-interesting topic of Quality Improvement vs. Research. What is the difference between QI and Research, and how do researchers and IRBs determine the difference between the two? Tiffany Gommel shares her experience, some helpful insights, and practical advice on this topic.  <br/><br/></p><p>Additional Resources: </p><ul><li>Example of QI vs Research Checklist from NIH - <a href='https://irbo.nih.gov/confluence/download/attachments/70321066/QA-QI%20vs.%20Research.pdf?version=1&amp;modificationDate=1645630780163&amp;api=v2'>https://irbo.nih.gov/confluence/download/attachments/70321066/QA-QI%20vs.%20Research.pdf?version=1&amp;modificationDate=1645630780163&amp;api=v2</a></li><li>Example guidance of QI vs Research from Icahn School of Medicine - <a href='https://researchroadmap.mssm.edu/other-research/cnri/ebp-qi-research/'>https://researchroadmap.mssm.edu/other-research/cnri/ebp-qi-research/</a></li><li>Learn more about HRP Consulting here - <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Tiffany Gommel, the Director of the Office of IRB Operations (IRBO) at the National Institutes of Health (NIH) for the Intramural Research Program, is responsible for the operation and support of the NIH IRB, which reviews and approves human subjects research from the 27 Institutes across the NIH. With over two decades of clinical research experience, Tiffany has valuable expertise running IRBs at multiple organizations.<br/><br/></p>]]></content:encoded>
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    <pubDate>Tue, 30 Jul 2024 09:00:00 -0400</pubDate>
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  <psc:chapter start="0:00" title="Quality Improvement vs. Research: What&#39;s the Difference? - On Research Podcast" />
  <psc:chapter start="3:39" title="Tiffany Gommel’s Background" />
  <psc:chapter start="4:28" title="Quality Improvement vs. Research" />
  <psc:chapter start="5:04" title="Defining Research" />
  <psc:chapter start="5:39" title="Defining Quality Improvement" />
  <psc:chapter start="7:05" title="Generalizability in Quality Improvement" />
  <psc:chapter start="8:21" title="Intent and Generalizability Discussion" />
  <psc:chapter start="10:29" title="Publishing Quality Improvement Findings" />
  <psc:chapter start="11:11" title="IRB Review and Publication" />
  <psc:chapter start="13:40" title="Nuances of Determining Quality Improvement" />
  <psc:chapter start="16:03" title="Process for Quality Improvement Projects" />
  <psc:chapter start="19:12" title="Comfort Level with IRB Decisions" />
  <psc:chapter start="21:56" title="Responsibility for Determining Project Type" />
  <psc:chapter start="23:10" title="Quality Improvement Trust" />
  <psc:chapter start="25:08" title="Starting a Quality Improvement Program" />
  <psc:chapter start="26:15" title="Post-Approval Monitoring Challenges" />
  <psc:chapter start="27:56" title="Advice for Research and IRB" />
  <psc:chapter start="28:24" title="Engaging with New Researchers" />
  <psc:chapter start="30:26" title="Diverse Educational Approaches" />
  <psc:chapter start="32:06" title="Same Team: Shared Experiences in Research" />
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    <itunes:title>The Evolution of IRBs: Navigating Ethical Considerations in Research - On Research Podcast</itunes:title>
    <title>The Evolution of IRBs: Navigating Ethical Considerations in Research - On Research Podcast</title>
    <itunes:summary><![CDATA[Join us for a thoughtful, long-form discussion about the evolving IRB Industry.  Julie Blasingim, the CEO of Univo IRB, sits down to talk about how we got to the current IRB landscape we have now, and the future of IRBs. She covers a lot of areas related to the IRB, including how for-profit IRBs balance ethical reviews with the economics of business, identifying the gap between patients and the IRB process, as well as some hot topics for the IRB, like growing privacy protection concerns ...]]></itunes:summary>
    <description><![CDATA[<p>Join us for a thoughtful, long-form discussion about the evolving IRB Industry.  Julie Blasingim, the CEO of Univo IRB, sits down to talk about how we got to the current IRB landscape we have now, and the future of IRBs. She covers a lot of areas related to the IRB, including how for-profit IRBs balance ethical reviews with the economics of business, identifying the gap between patients and the IRB process, as well as some hot topics for the IRB, like growing privacy protection concerns and the impact of AI on the IRB process. <br/> <br/><br/>Additional Resources: </p><ul><li>Learn more about Univo IRB: <a href='https://www.univo-group.com/'>https://www.univo-group.com/</a></li><li>NIH article about research populations - <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889234/ '>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889234/ </a></li><li>Learn more about HRP Consulting: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a><br/><br/></li></ul><p>Guest Bio: Julie Blasingim, CEO of Univo IRB, is a seasoned IRB executive with 20 years of extensive regulatory, operational, and compliance experience in human research protection and site operations of clinical research. She has served in a dozen senior leadership roles across multiple central IRBs, has hosted countless FDA inspections at both the IRB and under-site operations, and has managed multiple accreditations and certifications through AAHRPP and ISO. Julie holds a master’s degree in business administration specializing in leadership.    </p>]]></description>
    <content:encoded><![CDATA[<p>Join us for a thoughtful, long-form discussion about the evolving IRB Industry.  Julie Blasingim, the CEO of Univo IRB, sits down to talk about how we got to the current IRB landscape we have now, and the future of IRBs. She covers a lot of areas related to the IRB, including how for-profit IRBs balance ethical reviews with the economics of business, identifying the gap between patients and the IRB process, as well as some hot topics for the IRB, like growing privacy protection concerns and the impact of AI on the IRB process. <br/> <br/><br/>Additional Resources: </p><ul><li>Learn more about Univo IRB: <a href='https://www.univo-group.com/'>https://www.univo-group.com/</a></li><li>NIH article about research populations - <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889234/ '>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889234/ </a></li><li>Learn more about HRP Consulting: <a href='https://thehrpconsultinggroup.com/'>https://thehrpconsultinggroup.com/</a></li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a><br/><br/></li></ul><p>Guest Bio: Julie Blasingim, CEO of Univo IRB, is a seasoned IRB executive with 20 years of extensive regulatory, operational, and compliance experience in human research protection and site operations of clinical research. She has served in a dozen senior leadership roles across multiple central IRBs, has hosted countless FDA inspections at both the IRB and under-site operations, and has managed multiple accreditations and certifications through AAHRPP and ISO. Julie holds a master’s degree in business administration specializing in leadership.    </p>]]></content:encoded>
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    <pubDate>Tue, 25 Jun 2024 09:00:00 -0400</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="The Evolution of IRBs: Navigating Ethical Considerations in Research - On Research Podcast" />
  <psc:chapter start="1:02" title="Introduction to Julie Blasingim " />
  <psc:chapter start="1:42" title="Julie&#39;s Journey into the Research Industry " />
  <psc:chapter start="3:02" title="Evolution of Independent IRBs " />
  <psc:chapter start="7:09" title="IRB Landscape Changes " />
  <psc:chapter start="15:30" title="Managing Ethical Concerns in For-Profit " />
  <psc:chapter start="19:54" title="Disconnect Between IRBs and Patients " />
  <psc:chapter start="23:45" title="IRBs&#39; Unique Position " />
  <psc:chapter start="24:46" title="Patient-Centric Approach " />
  <psc:chapter start="26:14" title="IRBs&#39; Evolution" />
  <psc:chapter start="28:29" title="Ethical Concerns in Research " />
  <psc:chapter start="31:22" title="IT Security and IRB Boards " />
  <psc:chapter start="33:52" title="AI Impact on IRBs " />
  <psc:chapter start="40:10" title="Ethical Framework and Decision-Making" />
  <psc:chapter start="43:09" title="Balancing Risk and Patient Empowerment " />
  <psc:chapter start="46:37" title="Same Team: Impactful Research " />
  <psc:chapter start="48:57" title="Closing Remarks" />
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    <itunes:duration>2971</itunes:duration>
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  <item>
    <itunes:title>Improving Access to Research Studies - On Research Podcast</itunes:title>
    <title>Improving Access to Research Studies - On Research Podcast</title>
    <itunes:summary><![CDATA[Access to research is a complicated but essential area of growing concern in the research industry. As technology advances, many smaller research sites and rural areas can’t compete or keep up. By narrowing the field of eligible research participants, we lose important patient populations. Jessica Rowe, the Director of Quality and Education at the Yale Cancer Center and the current President of the Society of Clinical Research Professionals (SOCRA), joins me in discussing this fascinating top...]]></itunes:summary>
    <description><![CDATA[<p>Access to research is a complicated but essential area of growing concern in the research industry. As technology advances, many smaller research sites and rural areas can’t compete or keep up. By narrowing the field of eligible research participants, we lose important patient populations. Jessica Rowe, the Director of Quality and Education at the Yale Cancer Center and the current President of the Society of Clinical Research Professionals (SOCRA), joins me in discussing this fascinating topic.   </p><p>Additional Resources: </p><ul><li>Resources for increased access to research -  <a href='https://mrctcenter.org/'>https://mrctcenter.org/</a></li><li>Equitable Access to Clinical Trials: How Do We Achieve It? - <a href='https://ascopubs.org/doi/10.1200/EDBK_389838'>https://ascopubs.org/doi/10.1200/EDBK_389838</a></li><li>Learn more about the CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Jessica Rowe is the Quality and Education Director for the Yale Cancer Center Clinical Trials Office, where she oversees quality and education initiatives. Throughout her career, Jessica has held varying positions in the clinical research industry, focusing on quality, HRPP, and compliance. She is also the current President of the Society of Clinical Research Associates (SOCRA). </p>]]></description>
    <content:encoded><![CDATA[<p>Access to research is a complicated but essential area of growing concern in the research industry. As technology advances, many smaller research sites and rural areas can’t compete or keep up. By narrowing the field of eligible research participants, we lose important patient populations. Jessica Rowe, the Director of Quality and Education at the Yale Cancer Center and the current President of the Society of Clinical Research Professionals (SOCRA), joins me in discussing this fascinating topic.   </p><p>Additional Resources: </p><ul><li>Resources for increased access to research -  <a href='https://mrctcenter.org/'>https://mrctcenter.org/</a></li><li>Equitable Access to Clinical Trials: How Do We Achieve It? - <a href='https://ascopubs.org/doi/10.1200/EDBK_389838'>https://ascopubs.org/doi/10.1200/EDBK_389838</a></li><li>Learn more about the CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul><p><br/>Guest Bio: Jessica Rowe is the Quality and Education Director for the Yale Cancer Center Clinical Trials Office, where she oversees quality and education initiatives. Throughout her career, Jessica has held varying positions in the clinical research industry, focusing on quality, HRPP, and compliance. She is also the current President of the Society of Clinical Research Associates (SOCRA). </p>]]></content:encoded>
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    <pubDate>Tue, 28 May 2024 08:00:00 -0400</pubDate>
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    <itunes:episode>5</itunes:episode>
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  <item>
    <itunes:title>Navigating the Complexities of Research Security - On Research Podcast</itunes:title>
    <title>Navigating the Complexities of Research Security - On Research Podcast</title>
    <itunes:summary><![CDATA[Research security is about protecting the means, know-how, and products of U.S. research and development until they are ready to be shared. In 2021, the government issued a national presidential memorandum with updated requirements for institutions around research. Emily Bradford joins us to explain these new research security requirements and suggests how to grow or build a program to meet these updated requirements.   Additional Resources:  - The original National Security Presidential...]]></itunes:summary>
    <description><![CDATA[<p>Research security is about protecting the means, know-how, and products of U.S. research and development until they are ready to be shared. In 2021, the government issued a national presidential memorandum with updated requirements for institutions around research. Emily Bradford joins us to explain these new research security requirements and suggests how to grow or build a program to meet these updated requirements.  </p><p>Additional Resources: <br/>- The original National Security Presidential Memorandum 33 document:<br/><a href='https://trumpwhitehouse.archives.gov/presidential-actions/presidential-memorandum-united-states-government-supported-research-development-national-security-policy/'>https://trumpwhitehouse.archives.gov/presidential-actions/presidential-memorandum-united-states-government-supported-research-development-national-security-policy/</a><br/>- National Institute of Standards and Technology – Research Security Framework: <br/><a href='https://nvlpubs.nist.gov/nistpubs/ir/2023/NIST.IR.8484.pdf'>https://nvlpubs.nist.gov/nistpubs/ir/2023/NIST.IR.8484.pdf</a><br/>- Updated Policy Regarding Use of Common Disclosure Forms: <br/><a href='https://www.whitehouse.gov/wp-content/uploads/2024/02/OSTP-Common-Disclosure-Form-Policy.pdf'>https://www.whitehouse.gov/wp-content/uploads/2024/02/OSTP-Common-Disclosure-Form-Policy.pdf</a><br/>- CITI Program&apos;s Research Security Training Online Course: <a href='https://about.citiprogram.org/course/research-security-training/'>https://about.citiprogram.org/course/research-security-training/</a> <br/>- Learn more about CITI Program at: <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  <br/><br/>Guest Bio: Dr. Emily Bradford is the Assistant Director of Research Compliance at the University of Kentucky. Under the Office of Sponsored Projects, she oversees conflicts of interest, research security, export controls, and some aspects of clinical trial compliance. She was previously an assistant professor at the College of Medicine and has served on Animal Care and Use Committees as well as healthcare ethics committees. <br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p>Research security is about protecting the means, know-how, and products of U.S. research and development until they are ready to be shared. In 2021, the government issued a national presidential memorandum with updated requirements for institutions around research. Emily Bradford joins us to explain these new research security requirements and suggests how to grow or build a program to meet these updated requirements.  </p><p>Additional Resources: <br/>- The original National Security Presidential Memorandum 33 document:<br/><a href='https://trumpwhitehouse.archives.gov/presidential-actions/presidential-memorandum-united-states-government-supported-research-development-national-security-policy/'>https://trumpwhitehouse.archives.gov/presidential-actions/presidential-memorandum-united-states-government-supported-research-development-national-security-policy/</a><br/>- National Institute of Standards and Technology – Research Security Framework: <br/><a href='https://nvlpubs.nist.gov/nistpubs/ir/2023/NIST.IR.8484.pdf'>https://nvlpubs.nist.gov/nistpubs/ir/2023/NIST.IR.8484.pdf</a><br/>- Updated Policy Regarding Use of Common Disclosure Forms: <br/><a href='https://www.whitehouse.gov/wp-content/uploads/2024/02/OSTP-Common-Disclosure-Form-Policy.pdf'>https://www.whitehouse.gov/wp-content/uploads/2024/02/OSTP-Common-Disclosure-Form-Policy.pdf</a><br/>- CITI Program&apos;s Research Security Training Online Course: <a href='https://about.citiprogram.org/course/research-security-training/'>https://about.citiprogram.org/course/research-security-training/</a> <br/>- Learn more about CITI Program at: <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  <br/><br/>Guest Bio: Dr. Emily Bradford is the Assistant Director of Research Compliance at the University of Kentucky. Under the Office of Sponsored Projects, she oversees conflicts of interest, research security, export controls, and some aspects of clinical trial compliance. She was previously an assistant professor at the College of Medicine and has served on Animal Care and Use Committees as well as healthcare ethics committees. <br/><br/></p>]]></content:encoded>
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    <pubDate>Tue, 23 Apr 2024 10:00:00 -0400</pubDate>
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    <itunes:title>Understanding Exception from Informed Consent - On Research Podcast</itunes:title>
    <title>Understanding Exception from Informed Consent - On Research Podcast</title>
    <itunes:summary><![CDATA[A growing area of research involves exception from informed consent. In an emergency setting, participants can be enrolled in a trial without their consent. Mike Linke joins On Research to discuss the regulations and ethical considerations around this important area of research.       Additional Resources:    FDA Guidance Document for EFIC studies - https://www.fda.gov/regulatory-information/search-fda-guidance-documents/exception-informed-consent-requirements-emergency-re...]]></itunes:summary>
    <description><![CDATA[<p>A growing area of research involves exception from informed consent. In an emergency setting, participants can be enrolled in a trial without their consent. Mike Linke joins On Research to discuss the regulations and ethical considerations around this important area of research.   <br/> <br/><br/>Additional Resources: <br/><br/></p><ul><li>FDA Guidance Document for EFIC studies - <a href='https://www.fda.gov/regulatory-information/search-fda-guidance-documents/exception-informed-consent-requirements-emergency-research '>https://www.fda.gov/regulatory-information/search-fda-guidance-documents/exception-informed-consent-requirements-emergency-research </a></li><li>NIH Resources about EFIC studies - <a href='https://www.ninds.nih.gov/current-research/trans-agency-activities/office-emergency-care-research/research-involving-exception-informed-consent'>https://www.ninds.nih.gov/current-research/trans-agency-activities/office-emergency-care-research/research-involving-exception-informed-consent</a> </li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org  </a></li><li>Learn more about HRP Consulting at HRP Consulting Group (<a href='https://thehrpconsultinggroup.com/'>thehrpconsultinggroup.com</a>). </li></ul><p><br/>Guest Bio: Mike Linke is a scientist, researcher, and IRB Chair. He has been in the research industry for 30 years and serves as the StrokeNet IRB Chair and the SMART IRB Program Director for Education. Mike has extensive experience working with Exception from Informed Consent (EFIC) studies.  </p>]]></description>
    <content:encoded><![CDATA[<p>A growing area of research involves exception from informed consent. In an emergency setting, participants can be enrolled in a trial without their consent. Mike Linke joins On Research to discuss the regulations and ethical considerations around this important area of research.   <br/> <br/><br/>Additional Resources: <br/><br/></p><ul><li>FDA Guidance Document for EFIC studies - <a href='https://www.fda.gov/regulatory-information/search-fda-guidance-documents/exception-informed-consent-requirements-emergency-research '>https://www.fda.gov/regulatory-information/search-fda-guidance-documents/exception-informed-consent-requirements-emergency-research </a></li><li>NIH Resources about EFIC studies - <a href='https://www.ninds.nih.gov/current-research/trans-agency-activities/office-emergency-care-research/research-involving-exception-informed-consent'>https://www.ninds.nih.gov/current-research/trans-agency-activities/office-emergency-care-research/research-involving-exception-informed-consent</a> </li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org  </a></li><li>Learn more about HRP Consulting at HRP Consulting Group (<a href='https://thehrpconsultinggroup.com/'>thehrpconsultinggroup.com</a>). </li></ul><p><br/>Guest Bio: Mike Linke is a scientist, researcher, and IRB Chair. He has been in the research industry for 30 years and serves as the StrokeNet IRB Chair and the SMART IRB Program Director for Education. Mike has extensive experience working with Exception from Informed Consent (EFIC) studies.  </p>]]></content:encoded>
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    <pubDate>Tue, 26 Mar 2024 12:00:00 -0400</pubDate>
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  <psc:chapter start="0:00" title="Introduction to Research Ethics and Participant Care" />
  <psc:chapter start="0:22" title="Welcome to &#39;On Research with CIT Program&#39; Podcast" />
  <psc:chapter start="0:36" title="Legal Disclaimer and Purpose of the Podcast" />
  <psc:chapter start="0:55" title="Introducing Mike Link: A Veteran in Research and IRB Leadership" />
  <psc:chapter start="1:06" title="Exploring the Concept of Exception from Informed Consent (EFIC)" />
  <psc:chapter start="1:47" title="Mike&#39;s Journey: From Microbiologist to IRB Chair" />
  <psc:chapter start="3:36" title="Mike&#39;s Current Projects and Contributions Post-Retirement" />
  <psc:chapter start="5:08" title="Diving Deep into Exception from Informed Consent (EFIC)" />
  <psc:chapter start="9:41" title="Community Consultation and Public Disclosure in EFIC Studies" />
  <psc:chapter start="14:46" title="Adapting to Modern Communication Avenues for EFIC Studies" />
  <psc:chapter start="18:16" title="Navigating the Complexities of EFIC Studies" />
  <psc:chapter start="18:52" title="Public Perception and Acceptance of EFIC Studies" />
  <psc:chapter start="19:43" title="Withdrawal and Data Retention in EFIC Studies" />
  <psc:chapter start="20:25" title="Insights from the NIH Meeting on EFIC" />
  <psc:chapter start="21:42" title="Evaluating EFIC Regulations and Future Directions" />
  <psc:chapter start="25:20" title="Challenges and Considerations in EFIC Study Design" />
  <psc:chapter start="31:14" title="The Importance of Community Involvement in EFIC" />
  <psc:chapter start="31:46" title="Reflecting on a Career in Research and IRB" />
</psc:chapters>
    <itunes:duration>2128</itunes:duration>
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    <itunes:season>2</itunes:season>
    <itunes:episode>3</itunes:episode>
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  </item>
  <item>
    <itunes:title>Research Site Operations - On Research Podcast</itunes:title>
    <title>Research Site Operations - On Research Podcast</title>
    <itunes:summary><![CDATA[A discussion about research site operations. We talk about the different types of sites, different recruitment strategies, how DCTs impact dedicated research sites, and the financial impact technology brings to sites. Adam Roth, the Vice President of Site Services at CTI, shares his experience and insights into the site world.    Guest Bio: Adam Roth has been in the clinical research industry for over 25 years. He started out as a research coordinator, then manager. He moved into project...]]></itunes:summary>
    <description><![CDATA[<p>A discussion about research site operations. We talk about the different types of sites, different recruitment strategies, how DCTs impact dedicated research sites, and the financial impact technology brings to sites. Adam Roth, the Vice President of Site Services at CTI, shares his experience and insights into the site world.  <br/><br/>Guest Bio: Adam Roth has been in the clinical research industry for over 25 years. He started out as a research coordinator, then manager. He moved into project management at a CRO, then operations director at a central IRB and currently serves as the Vice President, Research Site Services at a phase 1-4 multi-specialty clinical research site. <br/><br/><br/>Additional Resources: </p><ul><li>Interested in participating in a clinical research study? - Sign up with CTI: <a href='https://www.ctifacts.com/research-center/participate-in-a-clinical-research-study'>https://www.ctifacts.com/research-center/participate-in-a-clinical-research-study</a> </li><li>Developing Clinical Trial Budgets, Considerations, and Best Practices: <a href='https://pharmanewsintel.com/'>pharmanewsintel.com</a></li><li>Learn more about CITI Program at: <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul>]]></description>
    <content:encoded><![CDATA[<p>A discussion about research site operations. We talk about the different types of sites, different recruitment strategies, how DCTs impact dedicated research sites, and the financial impact technology brings to sites. Adam Roth, the Vice President of Site Services at CTI, shares his experience and insights into the site world.  <br/><br/>Guest Bio: Adam Roth has been in the clinical research industry for over 25 years. He started out as a research coordinator, then manager. He moved into project management at a CRO, then operations director at a central IRB and currently serves as the Vice President, Research Site Services at a phase 1-4 multi-specialty clinical research site. <br/><br/><br/>Additional Resources: </p><ul><li>Interested in participating in a clinical research study? - Sign up with CTI: <a href='https://www.ctifacts.com/research-center/participate-in-a-clinical-research-study'>https://www.ctifacts.com/research-center/participate-in-a-clinical-research-study</a> </li><li>Developing Clinical Trial Budgets, Considerations, and Best Practices: <a href='https://pharmanewsintel.com/'>pharmanewsintel.com</a></li><li>Learn more about CITI Program at: <a href='https://about.citiprogram.org/'>about.citiprogram.org</a>.  </li></ul>]]></content:encoded>
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    <pubDate>Tue, 27 Feb 2024 09:00:00 -0500</pubDate>
    <itunes:duration>2519</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>2</itunes:episode>
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  </item>
  <item>
    <itunes:title>Research Compliance - On Research Podcast</itunes:title>
    <title>Research Compliance - On Research Podcast</title>
    <itunes:summary><![CDATA[Our guest this month is Kate Cohen, the Chief Compliance Officer at SIU Medicine in Illinois. Kate breaks down the concept of research compliance, sharing best practices and practical guidance. We dive into essential elements of a compliance research program, as well as how someone new to this side of the industry can take steps to break in and learn more.    Additional Resources:   Updated OIG Guidance with 7 Elements https://oig.hhs.gov/compliance/compliance-guidance/  HCCA C...]]></itunes:summary>
    <description><![CDATA[<p>Our guest this month is Kate Cohen, the Chief Compliance Officer at SIU Medicine in Illinois. Kate breaks down the concept of research compliance, sharing best practices and practical guidance. We dive into essential elements of a compliance research program, as well as how someone new to this side of the industry can take steps to break in and learn more. </p><p> </p><p>Additional Resources:  </p><ul><li>Updated OIG Guidance with 7 Elements <a href='https://oig.hhs.gov/compliance/compliance-guidance/'>https://oig.hhs.gov/compliance/compliance-guidance/</a>  </li><li>HCCA Conference 2024 Events - <a href='https://assets.hcca-info.org/portals/0/PDFs/Events/Brochures/hcca-2024-conferences-1pgad.pdf'>hcca-2024-conferences-1pgad.pdf (hcca-info.org)</a>  </li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a></li></ul>]]></description>
    <content:encoded><![CDATA[<p>Our guest this month is Kate Cohen, the Chief Compliance Officer at SIU Medicine in Illinois. Kate breaks down the concept of research compliance, sharing best practices and practical guidance. We dive into essential elements of a compliance research program, as well as how someone new to this side of the industry can take steps to break in and learn more. </p><p> </p><p>Additional Resources:  </p><ul><li>Updated OIG Guidance with 7 Elements <a href='https://oig.hhs.gov/compliance/compliance-guidance/'>https://oig.hhs.gov/compliance/compliance-guidance/</a>  </li><li>HCCA Conference 2024 Events - <a href='https://assets.hcca-info.org/portals/0/PDFs/Events/Brochures/hcca-2024-conferences-1pgad.pdf'>hcca-2024-conferences-1pgad.pdf (hcca-info.org)</a>  </li><li>Learn more about CITI Program at <a href='https://about.citiprogram.org/'>about.citiprogram.org</a></li></ul>]]></content:encoded>
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    <pubDate>Wed, 24 Jan 2024 08:00:00 -0500</pubDate>
    <itunes:duration>1907</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>1</itunes:episode>
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  </item>
  <item>
    <itunes:title>PRIM&amp;R 2023: Insights and Takeaways - On Research Podcast</itunes:title>
    <title>PRIM&amp;R 2023: Insights and Takeaways - On Research Podcast</title>
    <itunes:summary><![CDATA[This is a special edition of On Research with CITI Program. Guest hosted by Margaret Rankovic, Director of Content and Education at CITI Program, this podcast provides a recap, insights, and key takeaways from the recently concluded PRIM&amp;R 2023 conference. The panel includes the following from CITI Program leadership team: Bharat Krishna, SVP &amp; Managing Director; Jaime Arango, Vice President of Content and Education; Cid Gomes, Senior Director of Information Technology; and Gina Sulli...]]></itunes:summary>
    <description><![CDATA[<p>This is a special edition of On Research with CITI Program. Guest hosted by Margaret Rankovic, Director of Content and Education at CITI Program, this podcast provides a recap, insights, and key takeaways from the recently concluded PRIM&amp;R 2023 conference. The panel includes the following from CITI Program leadership team: Bharat Krishna, SVP &amp; Managing Director; Jaime Arango, Vice President of Content and Education; Cid Gomes, Senior Director of Information Technology; and Gina Sullivan, Director of Sales and Marketing. The panel shares their personal reflections and observations gained from the conference. Stay tuned to hear about emerging hot topics and key takeaways. We also cover tips for getting the most out of your conference attendance.<br/><br/>To learn more about CITI Program please visit: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p>]]></description>
    <content:encoded><![CDATA[<p>This is a special edition of On Research with CITI Program. Guest hosted by Margaret Rankovic, Director of Content and Education at CITI Program, this podcast provides a recap, insights, and key takeaways from the recently concluded PRIM&amp;R 2023 conference. The panel includes the following from CITI Program leadership team: Bharat Krishna, SVP &amp; Managing Director; Jaime Arango, Vice President of Content and Education; Cid Gomes, Senior Director of Information Technology; and Gina Sullivan, Director of Sales and Marketing. The panel shares their personal reflections and observations gained from the conference. Stay tuned to hear about emerging hot topics and key takeaways. We also cover tips for getting the most out of your conference attendance.<br/><br/>To learn more about CITI Program please visit: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p>]]></content:encoded>
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    <itunes:image href="https://storage.buzzsprout.com/5ztcwlnxv65b4sqsmuwr0hsuh0nl?.jpg" />
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    <pubDate>Mon, 18 Dec 2023 08:00:00 -0500</pubDate>
    <itunes:duration>1797</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>13</itunes:episode>
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  </item>
  <item>
    <itunes:title>Survey Research as a Method: Part 2 - On Research Podcast</itunes:title>
    <title>Survey Research as a Method: Part 2 - On Research Podcast</title>
    <itunes:summary><![CDATA[Dr. Matt Jans has been conducting and innovating surveys for almost 25 years. He is currently Lead Statistician for the National Health and Nutrition Examination Survey (NHANES) at the National Center for Health Statistics (NCHS).* His survey experience spans academic, government, and private sectors. He is an active member of the American Association for Public Opinion Research (AAPOR).  *The views and opinions expressed are those of Dr. Jans and not the Centers for Disease Control and Preve...]]></itunes:summary>
    <description><![CDATA[<p>Dr. Matt Jans has been conducting and innovating surveys for almost 25 years. He is currently Lead Statistician for the National Health and Nutrition Examination Survey (NHANES) at the National Center for Health Statistics (NCHS).* His survey experience spans academic, government, and private sectors. He is an active member of the American Association for Public Opinion Research (AAPOR). <br/>*The views and opinions expressed are those of Dr. Jans and not the Centers for Disease Control and Prevention or the National Center for Health Statistics.<br/><br/>Survey research is a dynamic method that transforms curiosity into actionable insights. Utilizing carefully crafted questionnaires, it navigates the intricate terrain of public opinion, illuminating trends and attitudes. A powerful tool in social sciences and business, surveys enable the systematic collection of data, providing a quantitative understanding of diverse subjects. From gauging customer satisfaction to unraveling societal trends, each survey is a snapshot capturing the nuances of human perspectives. Methodical and versatile, survey research is a compass, guiding decision-makers toward informed choices. With its ability to distill complex data into comprehensible patterns, survey research is a cornerstone in evidence-based decision-making.<br/><br/>If you found the survey research insights in this episode interesting and want to learn more about this topic, check out CITI Program’s online course, Survey Research: Design, Planning, Implementation, and Ethics, authored by Dr. Matt Jans and Zoe Padgett. This comprehensive resource offers an in-depth exploration of survey research design, implementation, analysis, and ethical considerations. <br/><br/>Learn more about CITI Program:<br/>-<a href=' https://about.citiprogram.org/ '> https://about.citiprogram.org/ </a><br/>- <a href='https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/'>https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/</a></p>]]></description>
    <content:encoded><![CDATA[<p>Dr. Matt Jans has been conducting and innovating surveys for almost 25 years. He is currently Lead Statistician for the National Health and Nutrition Examination Survey (NHANES) at the National Center for Health Statistics (NCHS).* His survey experience spans academic, government, and private sectors. He is an active member of the American Association for Public Opinion Research (AAPOR). <br/>*The views and opinions expressed are those of Dr. Jans and not the Centers for Disease Control and Prevention or the National Center for Health Statistics.<br/><br/>Survey research is a dynamic method that transforms curiosity into actionable insights. Utilizing carefully crafted questionnaires, it navigates the intricate terrain of public opinion, illuminating trends and attitudes. A powerful tool in social sciences and business, surveys enable the systematic collection of data, providing a quantitative understanding of diverse subjects. From gauging customer satisfaction to unraveling societal trends, each survey is a snapshot capturing the nuances of human perspectives. Methodical and versatile, survey research is a compass, guiding decision-makers toward informed choices. With its ability to distill complex data into comprehensible patterns, survey research is a cornerstone in evidence-based decision-making.<br/><br/>If you found the survey research insights in this episode interesting and want to learn more about this topic, check out CITI Program’s online course, Survey Research: Design, Planning, Implementation, and Ethics, authored by Dr. Matt Jans and Zoe Padgett. This comprehensive resource offers an in-depth exploration of survey research design, implementation, analysis, and ethical considerations. <br/><br/>Learn more about CITI Program:<br/>-<a href=' https://about.citiprogram.org/ '> https://about.citiprogram.org/ </a><br/>- <a href='https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/'>https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/</a></p>]]></content:encoded>
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    <itunes:image href="https://storage.buzzsprout.com/7azn2lqq1gh68xk4qnd4tebo0pdu?.jpg" />
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    <pubDate>Tue, 12 Dec 2023 09:00:00 -0500</pubDate>
    <itunes:duration>1453</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>12</itunes:episode>
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  </item>
  <item>
    <itunes:title>Survey Research as a Method: Part 1 - On Research Podcast</itunes:title>
    <title>Survey Research as a Method: Part 1 - On Research Podcast</title>
    <itunes:summary><![CDATA[Dr. Matt Jans has been conducting and innovating surveys for almost 25 years. He is currently Lead Statistician for the National Health and Nutrition Examination Survey (NHANES) at the National Center for Health Statistics (NCHS).* His survey experience spans academic, government, and private sectors. He is an active member of the American Association for Public Opinion Research (AAPOR).  *The views and opinions expressed are those of Dr. Jans and not the Centers for Disease Control and ...]]></itunes:summary>
    <description><![CDATA[<p>Dr. Matt Jans has been conducting and innovating surveys for almost 25 years. He is currently Lead Statistician for the National Health and Nutrition Examination Survey (NHANES) at the National Center for Health Statistics (NCHS).* His survey experience spans academic, government, and private sectors. He is an active member of the American Association for Public Opinion Research (AAPOR). <br/>*The views and opinions expressed are those of Dr. Jans and not the Centers for Disease Control and Prevention or the National Center for Health Statistics.</p><p>Survey research is a dynamic method that transforms curiosity into actionable insights. Utilizing carefully crafted questionnaires, it navigates the intricate terrain of public opinion, illuminating trends and attitudes. A powerful tool in social sciences and business, surveys enable the systematic collection of data, providing a quantitative understanding of diverse subjects. From gauging customer satisfaction to unraveling societal trends, each survey is a snapshot capturing the nuances of human perspectives. Methodical and versatile, survey research is a compass, guiding decision-makers toward informed choices. With its ability to distill complex data into comprehensible patterns, survey research is a cornerstone in evidence-based decision-making.<br/><br/>If you found the survey research insights in this episode interesting and want to learn more about this topic, check out CITI Program’s online course, <a href='https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/'><em>Survey Research: Design, Planning, Implementation, and Ethics</em></a>, authored by Dr. Matt Jans and Zoe Padgett. This comprehensive resource offers an in-depth exploration of survey research design, implementation, analysis, and ethical considerations. </p><p>Learn more about CITI Program: <br/>- <a href='https://about.citiprogram.org/ '>https://about.citiprogram.org/ </a><br/>- <a href='https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/'>https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/</a></p>]]></description>
    <content:encoded><![CDATA[<p>Dr. Matt Jans has been conducting and innovating surveys for almost 25 years. He is currently Lead Statistician for the National Health and Nutrition Examination Survey (NHANES) at the National Center for Health Statistics (NCHS).* His survey experience spans academic, government, and private sectors. He is an active member of the American Association for Public Opinion Research (AAPOR). <br/>*The views and opinions expressed are those of Dr. Jans and not the Centers for Disease Control and Prevention or the National Center for Health Statistics.</p><p>Survey research is a dynamic method that transforms curiosity into actionable insights. Utilizing carefully crafted questionnaires, it navigates the intricate terrain of public opinion, illuminating trends and attitudes. A powerful tool in social sciences and business, surveys enable the systematic collection of data, providing a quantitative understanding of diverse subjects. From gauging customer satisfaction to unraveling societal trends, each survey is a snapshot capturing the nuances of human perspectives. Methodical and versatile, survey research is a compass, guiding decision-makers toward informed choices. With its ability to distill complex data into comprehensible patterns, survey research is a cornerstone in evidence-based decision-making.<br/><br/>If you found the survey research insights in this episode interesting and want to learn more about this topic, check out CITI Program’s online course, <a href='https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/'><em>Survey Research: Design, Planning, Implementation, and Ethics</em></a>, authored by Dr. Matt Jans and Zoe Padgett. This comprehensive resource offers an in-depth exploration of survey research design, implementation, analysis, and ethical considerations. </p><p>Learn more about CITI Program: <br/>- <a href='https://about.citiprogram.org/ '>https://about.citiprogram.org/ </a><br/>- <a href='https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/'>https://about.citiprogram.org/course/survey-research-design-planning-implementation-and-ethics/</a></p>]]></content:encoded>
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    <pubDate>Wed, 15 Nov 2023 10:00:00 -0500</pubDate>
    <itunes:duration>881</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>11</itunes:episode>
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  </item>
  <item>
    <itunes:title>Research and FMLA: Building HR Relationships - On Research Podcast</itunes:title>
    <title>Research and FMLA: Building HR Relationships - On Research Podcast</title>
    <itunes:summary><![CDATA[Tanya Brown is the Senior Director, HR Consulting, Employee and Labor Relations at Vanderbilt University. She has 15 years of experience in Human Resources in many industries including the private sector, public sector, and higher education. Tanya currently leads a team of HR Consultants, who are the primary contact for leaders and employees across the university for matters related to human resources, and workers’ compensation and leave team. Tanya has a Bachelor’s of Arts in Social Sciences...]]></itunes:summary>
    <description><![CDATA[<p>Tanya Brown is the Senior Director, HR Consulting, Employee and Labor Relations at Vanderbilt University. She has 15 years of experience in Human Resources in many industries including the private sector, public sector, and higher education. Tanya currently leads a team of HR Consultants, who are the primary contact for leaders and employees across the university for matters related to human resources, and workers’ compensation and leave team. Tanya has a Bachelor’s of Arts in Social Sciences with a minor in Psychology from the University of Arizona and a Master’s of Science in Human Resources Strategic Management from Bellevue University.</p><p>The Family and Medical Leave Act (FMLA) is of paramount importance in a research setting. Researchers often face demanding workloads and unique challenges, and FMLA ensures they can balance their professional commitments with personal needs. This legislation grants eligible employees up to 12 weeks of unpaid, job-protected leave, enabling them to address critical family or health issues without risking their careers. In a research environment, where project continuity is essential, FMLA helps maintain ongoing work, minimizes disruptions, and fosters a more inclusive, supportive atmosphere. It promotes work-life balance, ensuring the well-being and productivity of researchers, thus contributing to the overall success of research endeavors.</p><p>Learn more about CITI Program: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p>]]></description>
    <content:encoded><![CDATA[<p>Tanya Brown is the Senior Director, HR Consulting, Employee and Labor Relations at Vanderbilt University. She has 15 years of experience in Human Resources in many industries including the private sector, public sector, and higher education. Tanya currently leads a team of HR Consultants, who are the primary contact for leaders and employees across the university for matters related to human resources, and workers’ compensation and leave team. Tanya has a Bachelor’s of Arts in Social Sciences with a minor in Psychology from the University of Arizona and a Master’s of Science in Human Resources Strategic Management from Bellevue University.</p><p>The Family and Medical Leave Act (FMLA) is of paramount importance in a research setting. Researchers often face demanding workloads and unique challenges, and FMLA ensures they can balance their professional commitments with personal needs. This legislation grants eligible employees up to 12 weeks of unpaid, job-protected leave, enabling them to address critical family or health issues without risking their careers. In a research environment, where project continuity is essential, FMLA helps maintain ongoing work, minimizes disruptions, and fosters a more inclusive, supportive atmosphere. It promotes work-life balance, ensuring the well-being and productivity of researchers, thus contributing to the overall success of research endeavors.</p><p>Learn more about CITI Program: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p>]]></content:encoded>
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    <pubDate>Tue, 24 Oct 2023 11:00:00 -0400</pubDate>
    <itunes:duration>753</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>10</itunes:episode>
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  </item>
  <item>
    <itunes:title>Life as an Unaffiliated IRB Member - On Research Podcast</itunes:title>
    <title>Life as an Unaffiliated IRB Member - On Research Podcast</title>
    <itunes:summary><![CDATA[In this special edition of the On Research with CITI Program podcast, we speak to Sally Mann about her role as an unaffiliated IRB member. Regulations in the U.S. and Canada include requirements associated with the membership of Institutional Review Boards (IRBs)/Research Ethics Boards (REBs). Both regulations require at least one member not to be otherwise affiliated with the institution. Serving as an unaffiliated IRB member is a challenging and rewarding experience.    Additional Resources...]]></itunes:summary>
    <description><![CDATA[<p>In this special edition of the On Research with CITI Program podcast, we speak to Sally Mann about her role as an unaffiliated IRB member.</p><p>Regulations in the U.S. and Canada include requirements associated with the membership of Institutional Review Boards (IRBs)/Research Ethics Boards (REBs). Both regulations require at least one member not to be otherwise affiliated with the institution. Serving as an unaffiliated IRB member is a challenging and rewarding experience.<br/><br/><br/></p><p>Additional Resources: </p><ul><li>45 CFR 46 – Protection of Human Subjects (<a href='https://www.ecfr.gov/on/2018-07-19/title-45/subtitle-A/subchapter-A/part-46'>https://www.ecfr.gov/on/2018-07-19/title-45/subtitle-A/subchapter-A/part-46</a>) </li><li>TCPS 2 (2002) – Chapter 1: Ethics Framework (<a href='https://ethics.gc.ca/eng/tcps2-eptc2_2022_chapter1-chapitre1.html#a'>https://ethics.gc.ca/eng/tcps2-eptc2_2022_chapter1-chapitre1.html#a</a>)</li><li>CITI Program module - I Have Agreed to be an IRB Community Member, Now What? (<a href='https://about.citiprogram.org/course/biomedical-biomed-basic/'>https://about.citiprogram.org/course/biomedical-biomed-basic/</a>)</li><li>Evolving Concern: Protection for Human Subjects (<a href='http://www.youtube.com/watch?v=_8Ku4b1fW18'>http://www.youtube.com/watch?v=_8Ku4b1fW18</a>) </li><li>Institutional Review Boards (<a href='http://www.youtube.com/watch?v=U8fme1boEbE'>http://www.youtube.com/watch?v=U8fme1boEbE</a>)</li></ul>]]></description>
    <content:encoded><![CDATA[<p>In this special edition of the On Research with CITI Program podcast, we speak to Sally Mann about her role as an unaffiliated IRB member.</p><p>Regulations in the U.S. and Canada include requirements associated with the membership of Institutional Review Boards (IRBs)/Research Ethics Boards (REBs). Both regulations require at least one member not to be otherwise affiliated with the institution. Serving as an unaffiliated IRB member is a challenging and rewarding experience.<br/><br/><br/></p><p>Additional Resources: </p><ul><li>45 CFR 46 – Protection of Human Subjects (<a href='https://www.ecfr.gov/on/2018-07-19/title-45/subtitle-A/subchapter-A/part-46'>https://www.ecfr.gov/on/2018-07-19/title-45/subtitle-A/subchapter-A/part-46</a>) </li><li>TCPS 2 (2002) – Chapter 1: Ethics Framework (<a href='https://ethics.gc.ca/eng/tcps2-eptc2_2022_chapter1-chapitre1.html#a'>https://ethics.gc.ca/eng/tcps2-eptc2_2022_chapter1-chapitre1.html#a</a>)</li><li>CITI Program module - I Have Agreed to be an IRB Community Member, Now What? (<a href='https://about.citiprogram.org/course/biomedical-biomed-basic/'>https://about.citiprogram.org/course/biomedical-biomed-basic/</a>)</li><li>Evolving Concern: Protection for Human Subjects (<a href='http://www.youtube.com/watch?v=_8Ku4b1fW18'>http://www.youtube.com/watch?v=_8Ku4b1fW18</a>) </li><li>Institutional Review Boards (<a href='http://www.youtube.com/watch?v=U8fme1boEbE'>http://www.youtube.com/watch?v=U8fme1boEbE</a>)</li></ul>]]></content:encoded>
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    <pubDate>Tue, 12 Sep 2023 15:00:00 -0400</pubDate>
    <itunes:duration>1810</itunes:duration>
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    <itunes:season>1</itunes:season>
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  <item>
    <itunes:title>Consent in Clinical Research - On Research Podcast</itunes:title>
    <title>Consent in Clinical Research - On Research Podcast</title>
    <itunes:summary><![CDATA[Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards,...]]></itunes:summary>
    <description><![CDATA[<p>Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards, policy maintenance and development, and training/mentoring of IRB staff. Linda formed IRB Consulting, LLC in 2012, providing IRB administrative services, training and education, audit services, and general consulting to numerous IRB programs nationwide.</p><p>According to the Food and Drug Administration, the purpose of clinical trials is to study medical products in people. In doing so, consent is critical in clinical trials for these people to understand they are the research subjects and not imply a patient. Consent within research ensures individuals have an informed choice on whether they want to participate in a research study. Informed consent within research is meant to protect human subjects from harm that could occur from participating in research and should always be voluntary.</p><p>Resources: </p><ul><li><a href='https://www.niaid.nih.gov/research/dmid-protocols-informed-consent'>https://www.niaid.nih.gov/research/dmid-protocols-informed-consent</a></li><li><a href='https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf'>https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf</a></li><li><a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/'>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/</a></li><li><a href='https://www.fda.gov/patients/clinical-trials-what-patients-need-know/informed-consent-clinical-trials'>https://www.fda.gov/patients/clinical-trials-what-patients-need-know/informed-consent-clinical-trials</a></li></ul>]]></description>
    <content:encoded><![CDATA[<p>Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards, policy maintenance and development, and training/mentoring of IRB staff. Linda formed IRB Consulting, LLC in 2012, providing IRB administrative services, training and education, audit services, and general consulting to numerous IRB programs nationwide.</p><p>According to the Food and Drug Administration, the purpose of clinical trials is to study medical products in people. In doing so, consent is critical in clinical trials for these people to understand they are the research subjects and not imply a patient. Consent within research ensures individuals have an informed choice on whether they want to participate in a research study. Informed consent within research is meant to protect human subjects from harm that could occur from participating in research and should always be voluntary.</p><p>Resources: </p><ul><li><a href='https://www.niaid.nih.gov/research/dmid-protocols-informed-consent'>https://www.niaid.nih.gov/research/dmid-protocols-informed-consent</a></li><li><a href='https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf'>https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf</a></li><li><a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/'>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/</a></li><li><a href='https://www.fda.gov/patients/clinical-trials-what-patients-need-know/informed-consent-clinical-trials'>https://www.fda.gov/patients/clinical-trials-what-patients-need-know/informed-consent-clinical-trials</a></li></ul>]]></content:encoded>
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    <pubDate>Tue, 15 Aug 2023 12:00:00 -0400</pubDate>
    <itunes:duration>1066</itunes:duration>
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    <itunes:season>1</itunes:season>
    <itunes:episode>8</itunes:episode>
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  <item>
    <itunes:title>Consent in Research - On Research Podcast</itunes:title>
    <title>Consent in Research - On Research Podcast</title>
    <itunes:summary><![CDATA[Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards,...]]></itunes:summary>
    <description><![CDATA[<p>Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards, policy maintenance and development, and training/mentoring of IRB staff. Linda formed IRB Consulting, LLC in 2012, providing IRB administrative services, training and education, audit services, and general consulting to numerous IRB programs nationwide.</p><p>Informed consent is critical and a main principle of research ethics in a research study. Consent within research ensures individuals have an informed choice on whether they want to participate in a research study. Informed consent applies to research in the social-behavioral, physical, and medical sciences. Informed consent within research is meant to protect human subjects from harm that could occur from participating in research and should always be voluntary.<br/><br/>Learn more about CITI Program: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p><p>Resources: </p><ul><li><a href='https://www.niaid.nih.gov/research/dmid-protocols-informed-consent'>https://www.niaid.nih.gov/research/dmid-protocols-informed-consent</a></li><li><a href='https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf'>https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf</a></li><li><a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/'>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/</a></li></ul><p><br/></p>]]></description>
    <content:encoded><![CDATA[<p>Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards, policy maintenance and development, and training/mentoring of IRB staff. Linda formed IRB Consulting, LLC in 2012, providing IRB administrative services, training and education, audit services, and general consulting to numerous IRB programs nationwide.</p><p>Informed consent is critical and a main principle of research ethics in a research study. Consent within research ensures individuals have an informed choice on whether they want to participate in a research study. Informed consent applies to research in the social-behavioral, physical, and medical sciences. Informed consent within research is meant to protect human subjects from harm that could occur from participating in research and should always be voluntary.<br/><br/>Learn more about CITI Program: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p><p>Resources: </p><ul><li><a href='https://www.niaid.nih.gov/research/dmid-protocols-informed-consent'>https://www.niaid.nih.gov/research/dmid-protocols-informed-consent</a></li><li><a href='https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf'>https://www.nsf.gov/bfa/dias/policy/docs/45cfr690.pdf</a></li><li><a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/'>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980471/</a></li></ul><p><br/></p>]]></content:encoded>
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    <pubDate>Wed, 05 Jul 2023 22:00:00 -0400</pubDate>
    <itunes:duration>844</itunes:duration>
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  <item>
    <itunes:title>Survey Research and Bots - On Research Podcast</itunes:title>
    <title>Survey Research and Bots - On Research Podcast</title>
    <itunes:summary><![CDATA[This episode discusses the impact of online bots on survey research, ethical considerations and implications of using bots in survey research, and potential benefits and unintended consequence. Myra Luna-Lucero, EdD, is the Research Compliance Director at Columbia University’s Teachers College. She spearheaded the College’s “Ethics &amp; Safety Amid Uncertainty” initiative and co-chaired the Research Compliance &amp; Safety Committee. She has also recently launched the “Research Writing &amp;...]]></itunes:summary>
    <description><![CDATA[<p>This episode discusses the impact of online bots on survey research, ethical considerations and implications of using bots in survey research, and potential benefits and unintended consequence.</p><p>Myra Luna-Lucero, EdD, is the Research Compliance Director at Columbia University’s Teachers College. She spearheaded the College’s “Ethics &amp; Safety Amid Uncertainty” initiative and co-chaired the Research Compliance &amp; Safety Committee. She has also recently launched the “Research Writing &amp; Ethics” internship program and oversaw an extensive transformation of the College’s IRB website. She regularly offers seminars and workshops on research compliance and IRB leadership. A researcher and teacher herself, Dr. Luna-Lucero has studied and published on student motivation in STEM fields, barriers to accessing education for students in rural communities, and community activism.</p><p>Learn more about CITI Program: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p><p>Resource: <a href='https://www.tc.columbia.edu/institutional-review-board/irb-blog/2022/bots-and-online-human-subjects-research/#:~:text=Researchers%20who%20use%20online%20platforms,posing%20as%20eligible%20human%20participants'>https://www.tc.columbia.edu/institutional-review-board/irb-blog/2022/bots-and-online-human-subjects-research/#:~:text=Researchers%20who%20use%20online%20platforms,posing%20as%20eligible%20human%20participants</a></p>]]></description>
    <content:encoded><![CDATA[<p>This episode discusses the impact of online bots on survey research, ethical considerations and implications of using bots in survey research, and potential benefits and unintended consequence.</p><p>Myra Luna-Lucero, EdD, is the Research Compliance Director at Columbia University’s Teachers College. She spearheaded the College’s “Ethics &amp; Safety Amid Uncertainty” initiative and co-chaired the Research Compliance &amp; Safety Committee. She has also recently launched the “Research Writing &amp; Ethics” internship program and oversaw an extensive transformation of the College’s IRB website. She regularly offers seminars and workshops on research compliance and IRB leadership. A researcher and teacher herself, Dr. Luna-Lucero has studied and published on student motivation in STEM fields, barriers to accessing education for students in rural communities, and community activism.</p><p>Learn more about CITI Program: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p><p>Resource: <a href='https://www.tc.columbia.edu/institutional-review-board/irb-blog/2022/bots-and-online-human-subjects-research/#:~:text=Researchers%20who%20use%20online%20platforms,posing%20as%20eligible%20human%20participants'>https://www.tc.columbia.edu/institutional-review-board/irb-blog/2022/bots-and-online-human-subjects-research/#:~:text=Researchers%20who%20use%20online%20platforms,posing%20as%20eligible%20human%20participants</a></p>]]></content:encoded>
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    <pubDate>Tue, 06 Jun 2023 12:00:00 -0400</pubDate>
    <itunes:duration>1199</itunes:duration>
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  <item>
    <itunes:title>Research Integrity - On Research Podcast</itunes:title>
    <title>Research Integrity - On Research Podcast</title>
    <itunes:summary><![CDATA[Ross Hickey is the Assistant Provost for Research Integrity at the University of Southern Maine (USM.) Ross is the Director of the Maine Regulatory Ethics and Training Center (MeRTEC) at USM. He is an attorney in Maine. His office serves institutions throughout the United States. Ross developed and teaches in the Regulatory Ethics undergraduate program at USM. He helped to develop and teaches in the compliance certificate program at Maine Law and also teaches there as an adjunct. He collabora...]]></itunes:summary>
    <description><![CDATA[<p>Ross Hickey is the Assistant Provost for Research Integrity at the University of Southern Maine (USM.) Ross is the Director of the Maine Regulatory Ethics and Training Center (MeRTEC) at USM. He is an attorney in Maine. His office serves institutions throughout the United States. Ross developed and teaches in the Regulatory Ethics undergraduate program at USM. He helped to develop and teaches in the compliance certificate program at Maine Law and also teaches there as an adjunct. He collaborates with universities in the North Atlantic, such as Iceland and Norway. He sits on the World Affairs Council for Maine.</p><p>Research integrity deals with the “best practices” or rules of professional practice or researchers. The United States National Institutes of Health expands on research integrity by stating it is “the use of honest and verifiable methods in proposing, performing, and evaluating research; reporting research results with particular attention to adherence to rules, regulations, guidelines, and following commonly accepted professional codes or norms.” (From:  <a href='https://grants.nih.gov/policy/research_integrity/what-is.htm#:~:text=the%20use%20of%20honest%20and,accepted%20professional%20codes%20or%20norms'>https://grants.nih.gov/policy/research_integrity/what-is.htm#:~:text=the%20use%20of%20honest%20and,accepted%20professional%20codes%20or%20norms</a>.) <br/>Responsible conduct of research (RCR) training is an essential component of any research project, regardless of a researcher’s source of funding.</p><p>Learn more about CITI Program: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p><p><br/></p>]]></description>
    <content:encoded><![CDATA[<p>Ross Hickey is the Assistant Provost for Research Integrity at the University of Southern Maine (USM.) Ross is the Director of the Maine Regulatory Ethics and Training Center (MeRTEC) at USM. He is an attorney in Maine. His office serves institutions throughout the United States. Ross developed and teaches in the Regulatory Ethics undergraduate program at USM. He helped to develop and teaches in the compliance certificate program at Maine Law and also teaches there as an adjunct. He collaborates with universities in the North Atlantic, such as Iceland and Norway. He sits on the World Affairs Council for Maine.</p><p>Research integrity deals with the “best practices” or rules of professional practice or researchers. The United States National Institutes of Health expands on research integrity by stating it is “the use of honest and verifiable methods in proposing, performing, and evaluating research; reporting research results with particular attention to adherence to rules, regulations, guidelines, and following commonly accepted professional codes or norms.” (From:  <a href='https://grants.nih.gov/policy/research_integrity/what-is.htm#:~:text=the%20use%20of%20honest%20and,accepted%20professional%20codes%20or%20norms'>https://grants.nih.gov/policy/research_integrity/what-is.htm#:~:text=the%20use%20of%20honest%20and,accepted%20professional%20codes%20or%20norms</a>.) <br/>Responsible conduct of research (RCR) training is an essential component of any research project, regardless of a researcher’s source of funding.</p><p>Learn more about CITI Program: <a href='https://about.citiprogram.org/'>https://about.citiprogram.org/</a></p><p><br/></p>]]></content:encoded>
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    <pubDate>Tue, 02 May 2023 16:00:00 -0400</pubDate>
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  <item>
    <itunes:title>What is an IRB Administrator- On Research Podcast</itunes:title>
    <title>What is an IRB Administrator- On Research Podcast</title>
    <itunes:summary><![CDATA[Cecilia Brooke Cholka serves Weill Cornell Medicine as a Human Research and QA Manager and consultant for the PEER Consulting Group. She works to demystify IRB processes and expectations so that researchers and the IRB can work together collaboratively to ensure ethical conduct of research. An Institutional Review Board or IRB is commonly found at institutions that conduct or participate in research activities. The purpose of the IRB is to evaluate research ethics by reviewing research method...]]></itunes:summary>
    <description><![CDATA[<p>Cecilia Brooke Cholka serves Weill Cornell Medicine as a Human Research and QA Manager and consultant for the PEER Consulting Group. She works to demystify IRB processes and expectations so that researchers and the IRB can work together collaboratively to ensure ethical conduct of research.</p><p>An Institutional Review Board or IRB is commonly found at institutions that conduct or participate in research activities. The purpose of the IRB is to evaluate research ethics by reviewing research methods related to their potential harm to different groups. An IRB Administrator is an individual who oversees and manages systems, structures, and operations of the IRB related to policy, process, procedures, and records.</p><p>Learn more about CITI Program: https://about.citiprogram.org/</p>]]></description>
    <content:encoded><![CDATA[<p>Cecilia Brooke Cholka serves Weill Cornell Medicine as a Human Research and QA Manager and consultant for the PEER Consulting Group. She works to demystify IRB processes and expectations so that researchers and the IRB can work together collaboratively to ensure ethical conduct of research.</p><p>An Institutional Review Board or IRB is commonly found at institutions that conduct or participate in research activities. The purpose of the IRB is to evaluate research ethics by reviewing research methods related to their potential harm to different groups. An IRB Administrator is an individual who oversees and manages systems, structures, and operations of the IRB related to policy, process, procedures, and records.</p><p>Learn more about CITI Program: https://about.citiprogram.org/</p>]]></content:encoded>
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    <pubDate>Tue, 04 Apr 2023 13:00:00 -0400</pubDate>
    <itunes:duration>1077</itunes:duration>
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  <item>
    <itunes:title>Artificial Intelligence in Research - On Research Podcast</itunes:title>
    <title>Artificial Intelligence in Research - On Research Podcast</title>
    <itunes:summary><![CDATA[Chirag Shah, Ph.D.,  is a Professor of Information and Computer Science at the University of Washington. He is the Founding Director of InfoSeeking Lab and Founding Co-Director of the Center for Responsibility in AI Systems &amp; Experiences (RAISE). He works on intelligent information access systems with a focus on fairness and transparency. Artificial intelligence, or AI, is utilized more and more frequently in different settings, including research. AI can be utilized within research ...]]></itunes:summary>
    <description><![CDATA[<p>Chirag Shah, Ph.D.,  is a Professor of Information and Computer Science at the University of Washington. He is the Founding Director of InfoSeeking Lab and Founding Co-Director of the Center for Responsibility in AI Systems &amp; Experiences (RAISE). He works on intelligent information access systems with a focus on fairness and transparency.</p><p>Artificial intelligence, or AI, is utilized more and more frequently in different settings, including research. AI can be utilized within research by optimizing resources, data, and technology to synthesize and analyze data or problems. With AI in research, so much is still unknown. How do you inform participants of informed consent and protect their data when utilizing AI? How do researchers account for bias or deception while utilizing AI in a research setting? Chirag Shah, Ph.D., discusses these issues and much more on this episode of On Research.</p><p>Learn more about CITI Program: https://about.citiprogram.org/</p>]]></description>
    <content:encoded><![CDATA[<p>Chirag Shah, Ph.D.,  is a Professor of Information and Computer Science at the University of Washington. He is the Founding Director of InfoSeeking Lab and Founding Co-Director of the Center for Responsibility in AI Systems &amp; Experiences (RAISE). He works on intelligent information access systems with a focus on fairness and transparency.</p><p>Artificial intelligence, or AI, is utilized more and more frequently in different settings, including research. AI can be utilized within research by optimizing resources, data, and technology to synthesize and analyze data or problems. With AI in research, so much is still unknown. How do you inform participants of informed consent and protect their data when utilizing AI? How do researchers account for bias or deception while utilizing AI in a research setting? Chirag Shah, Ph.D., discusses these issues and much more on this episode of On Research.</p><p>Learn more about CITI Program: https://about.citiprogram.org/</p>]]></content:encoded>
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    <pubDate>Tue, 07 Mar 2023 15:00:00 -0500</pubDate>
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    <itunes:title>Graduate Research and Controversial Topics - On Research Podcast</itunes:title>
    <title>Graduate Research and Controversial Topics - On Research Podcast</title>
    <itunes:summary><![CDATA[Lou Kavar is a faculty member in psychology at Capella University where he is the lead faculty member for qualitative research and teaches doctoral-level graduate courses in psychology. Lou has taught in higher education at the graduate level for over thirty years. His personal research interest is the integration of spirituality and psychology. He lives in Atlanta, GA. For more information on Lou's writing and work in the area of spirituality, visit his website: loukavar.com. Graduate studen...]]></itunes:summary>
    <description><![CDATA[<p>Lou Kavar is a faculty member in psychology at Capella University where he is the lead faculty member for qualitative research and teaches doctoral-level graduate courses in psychology. Lou has taught in higher education at the graduate level for over thirty years. His personal research interest is the integration of spirituality and psychology. He lives in Atlanta, GA. For more information on Lou&apos;s writing and work in the area of spirituality, visit his website: loukavar.com.</p><p>Graduate students at research institutions in the United States are often required to complete a major research project, such as a thesis or dissertation prior to graduation. In these research projects, graduate students might choose to research what one could deem as a controversial topic. Some topics that might be seen as controversial often include topics that involve religion, sex, gender, race, ethnicity, and other topics. Specifically in qualitative research, the researcher should be aware and consider the insider-outsider perspective prior to beginning their research. For graduate students, they should consult with their graduate or research advisor when engaging in research activities involving controversial topics.</p><p>Learn more about CITI Program: https://about.citiprogram.org/</p>]]></description>
    <content:encoded><![CDATA[<p>Lou Kavar is a faculty member in psychology at Capella University where he is the lead faculty member for qualitative research and teaches doctoral-level graduate courses in psychology. Lou has taught in higher education at the graduate level for over thirty years. His personal research interest is the integration of spirituality and psychology. He lives in Atlanta, GA. For more information on Lou&apos;s writing and work in the area of spirituality, visit his website: loukavar.com.</p><p>Graduate students at research institutions in the United States are often required to complete a major research project, such as a thesis or dissertation prior to graduation. In these research projects, graduate students might choose to research what one could deem as a controversial topic. Some topics that might be seen as controversial often include topics that involve religion, sex, gender, race, ethnicity, and other topics. Specifically in qualitative research, the researcher should be aware and consider the insider-outsider perspective prior to beginning their research. For graduate students, they should consult with their graduate or research advisor when engaging in research activities involving controversial topics.</p><p>Learn more about CITI Program: https://about.citiprogram.org/</p>]]></content:encoded>
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    <pubDate>Tue, 07 Feb 2023 16:00:00 -0500</pubDate>
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    <itunes:title>What is a Clinical Research Associate? - On Research Podcast</itunes:title>
    <title>What is a Clinical Research Associate? - On Research Podcast</title>
    <itunes:summary><![CDATA[Elizabeth Waddell, has over 20 years in the clinical research industry and is the owner of The CRA Helper. Elizabeth began her clinical research career as an in-house Clinical Research Associate (CRA) and later transitioned to an on-site CRA. Later in her career, she moved into a Line Manager role that focused on training new CRAs prior to launching her own company, The CRA Helper. What is a Clinical Research Associate (CRA)? A Clinical Research Associate or CRA is a professional within a hea...]]></itunes:summary>
    <description><![CDATA[<p>Elizabeth Waddell, has over 20 years in the clinical research industry and is the owner of The CRA Helper. Elizabeth began her clinical research career as an in-house Clinical Research Associate (CRA) and later transitioned to an on-site CRA. Later in her career, she moved into a Line Manager role that focused on training new CRAs prior to launching her own company, The CRA Helper.</p><p>What is a Clinical Research Associate (CRA)? A Clinical Research Associate or CRA is a professional within a healthcare setting who oversees research activities, typically related to clinical trials. CRAs can be employed and work in a variety of sectors, including government agencies, pharmaceutical companies, research institutions, and in similar settings. Most CRAs possess an academic degree from a higher education institution in a field related to the healthcare industry. The overall role and tasks of a CRA are outlined and defined by good clinical practice guidelines for clinical trials.</p><p>Learn more about CITI Program: https://about.citiprogram.org/</p>]]></description>
    <content:encoded><![CDATA[<p>Elizabeth Waddell, has over 20 years in the clinical research industry and is the owner of The CRA Helper. Elizabeth began her clinical research career as an in-house Clinical Research Associate (CRA) and later transitioned to an on-site CRA. Later in her career, she moved into a Line Manager role that focused on training new CRAs prior to launching her own company, The CRA Helper.</p><p>What is a Clinical Research Associate (CRA)? A Clinical Research Associate or CRA is a professional within a healthcare setting who oversees research activities, typically related to clinical trials. CRAs can be employed and work in a variety of sectors, including government agencies, pharmaceutical companies, research institutions, and in similar settings. Most CRAs possess an academic degree from a higher education institution in a field related to the healthcare industry. The overall role and tasks of a CRA are outlined and defined by good clinical practice guidelines for clinical trials.</p><p>Learn more about CITI Program: https://about.citiprogram.org/</p>]]></content:encoded>
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    <pubDate>Tue, 10 Jan 2023 09:00:00 -0500</pubDate>
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