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Previous Monthly Research Seminars
Note that some MediaSite presentations below require a UMID login.
| Date | Topic/Speaker | Archived Material(s) |
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November 2024 |
A Regulatory Binder QA Journey Casey Jackson, MS, CCRP |
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October 2024 |
Scary Compliance |
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September 2024 |
Informed Consent Approaches In Human Subjects Research Casey Jackson, MS, CCRP |
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August 2024 |
The Changing Ethics of Informed Consent and Biospecimens in Clinical Research Casey Snoddy, BS, CCRP |
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June 2024 |
Exemption and Risk Determination in Human Research Using Devices Donna Headlee, RN, BSN, CCRP |
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May 2024 |
The Voice of the Research Participant Jeffrey Wells |
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March 2024 |
Joint UMSON MRS and Baltimore SOCRA Chapter Meeting: SOP on SOPs Aryn Knight, BS, CCRP |
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February 2024 |
Community-Based Participatory Research in Action: Lessons Learned from an Academic-Community Collaboration Doris Titus-Glover, PhD, RN |
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January 2024 |
"Navigating the “IRB” When You're Not Doing Research" Casey Jackson, MS, CCRP |
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November 2023 |
"Pragmatic Clinical Trials: Research in the 'Real-World'”
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October |
"Navigating the Single IRB Process" Nichelle Cobb, PhD Michael Linke, PhD, CIP Polly Goodman, CIP |
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| September 2023 |
"Research Integrity and Scientific Misconduct" Kaylin A. Adipietro, PhD |
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| August 2023 |
“Research Participant Payment Considerations” James Campbell, MD, MS |
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| June 2023 |
"Research Record Retention & Destruction: Tips and Best Practices" Casey Jackson, MS, CCRP |
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| April 2023 |
"Trust in Research Using Digital Devices" Katie Shilton, PhD, associate professor and program co-director of the B.S. in Social Data Science, University of Maryland, College Park |
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| March 2023 |
"UMB Office of Accountability IRB/HRPO Related Audits" Sarah N. Archibald, PhD, MSL, MS, MDE, MA, CCEP Director, Auditing & Monitoring, Program Director, Research Administration Certificate Program |
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| February 2023 |
"FERPA and Research" Stephanie Suerth, MPA, CCEP Julie Doherty, DM, MSN, RN, CIP, CCEP |
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| January 2022 |
"NIH Data Sharing Policy" Taunton Paine, MA Director, Scientific Data Sharing Policy Division |
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| November 2022 |
"Smart IRB Process and External IRB Reliance at UMB" Julie Doherty DM, MSN, RN, CIP, CCEP |
Watch Doherty's presentation |
| October 2022 |
"HIPPA Security and Privacy of Data, with a Special Focus on Research" Peter Murray, PhD, CAS, MS |
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| September 2022 |
"Storytelling in Research" David O. Fakunle, PhD |
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| August 2022 |
"Online Research Best Practices" Christina L. Wright, MA, CIP Chiara Acquati, PhD, LMSW |
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| June 2022 |
"Qualitative Research and the IRB: A Primer for Researchers" Patricia Condon, PhD Andrew Hedrick, MPA, CIP |
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| May 2022 |
"Community Based Participatory Research: Challenges and Rewards" Julie Doherty, DM, MSN Robert E. Rosenthal, MD |
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| April 2022 |
"Research Consent Part 7: Electronic consent - what is it and what is it not?" Casey Jackson, MS, CCRP |
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| March 2022 |
"Research Consent Part 6: Regulatory & Ethical Considerations (Vulnerable Populations, assents, and short form consents)" Jon Mark Hirshon, MD, MPH, PhD |
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| February 2022 |
"Research Consent Part 5: Informed Consent in Human Subjects Research: Untangling Consent Waivers" Casey Jackson MS, CCRP |
Download Jackson's presentation slides. |
| January 2022 |
"Clinicaltrials.gov: All you need to know" Anthony Keyes, MBA, PMP |
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| November 2021 |
"Research Consent Part 4: Informed Consent in Human Subjects Research: Tips and Guidance on Consent Writing at UMB" Casey Jackson, MS, CCRP |
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| October 2021 |
"Research Consent Part 3: Integrating Health Literacy into the Informed Consent Process: Tips for Developing Understandable Consent Materials" Sylvia Baedorf Kassis, MPH |
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| September 2021 |
"Why should we care about protecting human research participates and how can we do it well?" Marianna Azar |
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| August 2021 |
"Research Consent Part 2: Required Elements of Consent" Jan Martinez, MS, CIP, CLSSGB Casey Jackson MS, CCRP |
Watch Martinez and Jackson's presentation (part 2) Download Martinez and Jackson's presentation slides (part 2). |
| June 2021 |
"Research Consent Part 1: History, Application, and Process" Jan Martinez, MS, CIP, CLSSGB Casey Jackson, MS, CCRP |
Watch Martinez and Jackson's presentation (part 1) Download Martinez and Jackson's presentation slides (part 1). |
| May 2021 |
"Site and Staff Engagement: Resources and Guidance for Understanding Who is Engaged in Your Human Subjects Research Protocol" Casey Jackson, MS, CCRP |
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| April 2021 |
"DocuSign Use for Research Compliant e-Signature Capture" Douglas Bowser Eunissa Yancy |
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| March 2021 |
"Reportable New Information (RNI) - What UMB Researchers NEED to Know" Julie Doherty, DM, MSN, RN, CIP, CCEP |
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| February 2021 |
"Auditing Human Subject Research" LaToya Lewis, MS, MT (ASCP), CCRP, CCEP |
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| January 2021 |
“Pediatric Research” James D. Campbell, MD, MS |
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| October 2020 |
"QI vs. Research" Casey Jackson, MS, CCRP |
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| September 2020 |
"Conflicts of Interest in Research" Alison J. Watkins, JD, MS |
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| August 2020 |
"Is my study exempt? Understanding exemption criteria" Jessica Rowe, MA, MS, CCRP |
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| June 2020 |
"Applying the 10th Principle of Good Clinical Practice (GCP): Good Data and Record Management Practices" Casey Jackson, MS, CCRP |
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| May 2020 |
"Non-Human Subjects Research Determinations" Maria Drayton, BS |
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| April 2020 |
"Best Practices for Research Data Management" Jean-Paul Courneya Amy Yarnell |
Watch Courneya and Yarnell's presentation Download Courneya and Yarnell's presentation slides. Download Courneya and Yarnell's handout. |
| Feb. 2020 |
"Lean Six Sigma in Research: Process Improvement, Minimizing Waste, CAPAs, and More" Emma Barkman, MHA, CCRP |
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| Jan. 2020 |
"HIPAA Awareness" Kent Buckingham |
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| Nov. 2019 |
"Preventing and Investigating Research Misconduct" Stephan Vigues, PhD |
Watch Vigues' presentation. |
| Oct. 17, 2019 |
"Conducting Research with Pediatric Populations" James D. Campbell, MD, MS |
Watch Campbell's presentation. View Campbell's presentation slides. |
| Sept. 19, 2019 |
"Developing Better Consent Forms" Everly Brown, MLIS Michele Nance, MS |
View Brown and Nance's presentation slides. |
| August 15, 2019 |
"Human Research Protections Program sIRB Processes & Workflow: Relying on an External IRB" Julie Doherty, DM, MSN, RN, CIP, CCEP |
View Doherty's presentation slides. |
| June 20, 2019 |
"Informed Consent and Ethical Considerations in Clinical Trials" |
View Hirshon's presentation slides. |
| May 16, 2019 |
"Conducting Research with Pediatric Populations" |
This lecture was not recorded. |
| April 22, 2019 | "Research Involving Participants with Diminished Capacity to Consent" Leslie I. Katzel, MD, PhD Associate Professor Baltimore VA Medical Center |
Watch Katzel's presentation. |
| March 28, 2019 |
"Applying the Revised Common Rule to Nursing Research" Jessica Rowe, MA, MS, CCRP |
This lecture was not recorded. |
| Feb. 12, 2019 | "Ensuring Institutional Compliance with Clinicaltrials.gov " Antony Keyes, MBA, PMP Aliya Lalji, MD Johns Hopkins University School of Medicine |
Watch Keyes and Lalji's presentation. |
| Jan. 17, 2019 |
"My Collaborator’s Keeper: When You Can Be Held Responsible for the Misconduct of Others" |
Watch Archibald's presentation. |
| Nov. 15, 2018 |
"Continuous Stakeholder Engagement in Research" |
Watch Edwards' presentation. |
| Oct. 18, 2018 |
"Conducting VA research" |
View Ivey's presentation slides. |
| Sept. 20, 2018 |
"Quality Management in Behavior Research" |
Watch Rowe's presentation. |
| Aug. 16, 2018 |
"Demystifying Expedited Event Reporting in Clinical Research" |
Watch Ness' presentation. |
| June 21, 2018 |
"FERPA and Research: The Other Privacy Law" |
Watch Suerth's presentation. (Note that the presentation cuts out in some areas.) |
| May 17, 2018 |
"Data Safety Monitoring in Human Subjects Research: Using Oversight to Avoid Oversights" |
Watch Luthardt's presentation. |
| April 19, 2018 |
"Navigating the Changing Regulatory Landscape- How the Common Rule Changes Will Impact You" |
Watch Williams' presentation. (Note that sound is unavailable.) |
| April 11, 2018 |
"Back to Basics: Informed Consent in Human Subjects Research" |
Watch Rowe's presentation. |
| March 15, 2018 |
"Protocol Development: A Practical Approach" |
Watch Palmer's presentation. |
| Feb. 15, 2018 | "Quality in Good Clinical Practice" Anita Moore, MS, RN, Nurse Consultant Centers for Medicare & Medicaid Services Quality, Safety, & Education Division |
View Moore's presentation slides. |
| Jan. 18, 2018 | "Research Misconduct in Human Subjects Research" Sarah N. Archibald, PhD, MS, MA, CCEP Research Integrity Officer Program Director, Research Integrity Office of Accountability and Compliance University of Maryland, Baltimore |
Watch Archibald's presentation. |
| Oct. 19, 2017 | "Ethics of Biobanking" Robert Rosenthal, MD Professor and Institutional Review Board Chair University of Maryland, Baltimore |
Watch Rosentha's presentation. |
| Sept. 14, 2017 | "Nonhuman Subjects, Exempt, and Expedited Research: What YOU Need to Know" Tara Catanzariti, IRB Administrator Human Research Protections Program University of Maryland, Baltimore |
Watch Catanzariti's presentation. |
| Aug. 17, 2017 | "HS/HSL Research Data Management Services and Data Management Essentials" Katherine Downton, MSLIS, AHIP Head of Research, Education and Outreach Services Health Sciences & Human Services Library University of Maryland, Baltimore Brian Zelip, MA, MS, Emerging Technologies Librarian Health Sciences & Human Services Library University of Maryland, Baltimore |
Watch Downton and Zelip's presentation. |
| June 15, 2017 | "Health Survey Research Methods" Presented by Jessica Brown, PhD Assistant Professor, University of Maryland School of Medicine |
Watch Brown's presentation. |
| May 18, 2017 | "Revised Common Rule: Major Changes to Expect" Presented by Monique Hawkins, MS, CIP Human Research Protection Administrator Department of the Navy Human Research Protection Program Warfighter Performance Science & Technology Department Office of Naval Research |
View Hawkins' presentation slides. |
| April 20, 2017 | "Reportable New Information: What You NEED to Know" Presented by Julie Doherty Director, Office of Academic Affairs, Human Research Protections Office University of Maryland, Baltimore |
Watch Doherty's presentation. |
| March 16, 2017 | "Conducting Research with Prisoners" Presented by Sarah Archibald, PhD, MS, MA, CCEP Research Integrity Officer Program Director, Research Integrity Office of Accountability and Compliance University of Maryland, Baltimore |
Watch Archibald's presentation. |
| Feb. 16, 2017 | "Considerations in Social Behavioral Research" Seth Himelhoch, MD, MPH |
Watch Himelhock's presentation. |
| Feb. 8, 2017 | "Issues of Authorship: Past, Present and Future" Adam Puche, PhD Presented as part of the Office of Accountability and Compliance Lecture Series Co-Sponsored by the Office of Research and Scholarship, UMSON, and the Research Career Development Program, UMSOM |
Watch Puche's presentation. |
| Jan. 19, 2017 | "Fostering Responsible Conduct of Research" presented by Adil Shamoo, PhD University of Maryland School of Medicine |
Watch Shamoo's presentation. |
| Nov. 17, 2016 | "UMB Research Integrity Office: What We Do and How We Do It" Stephan Vigues, PhD Accountability and Compliance, Research Integrity Office |
Watch Vigues' presentation. |
| Oct. 20, 2016 | "Children in Clinical Research: Ethical and Regulatory Considerations in Pediatrics" James Campbell, MD MS University of Maryland School of Medicine |
Watch Campbell's presentation. |
| Sept. 15, 2016 | Sept. 15, 2016 "Visualizing Data Integrity and Management through the Lens of Transparency" C.S. Raman, PhD, Associate Professor University of Maryland School of Pharmacy, Department of Pharmaceutical Sciences |
Watch Raman's presentation. View Raman's presentation slides. |
| Aug. 18, 2016 | "Consent or Not to Consent? That is the Question. Ethical Issues in Human Participant Research" Jon Mark Hirshon, MD, MPH, PhD University of Maryland, Baltimore |
Watch Hirshon's presentation. |
| June 16, 2016 | "What’s So Essential About Essential Documents? The Regulatory File" Jessica Rowe, MA, MS, CCRP UMSON Office of Research and Scholarship |
Watch Rowe's presentation. |
| May 12, 2016 | "Clinical Research Data Management" Elizabeth Ness, MS, RN Center for Cancer Research |
Watch Ness' presentation. |
| April 21, 2016 | "Research Misconduct" Sarah N. Archibald, PhD Research Integrity Officer University of Maryland, Baltimore |
Watch Archibald's presentation. |
| March 24, 2016 | "Proposed Changes to the Common Rule: What Does it All Mean?" Madeleine Williams, Huron Consulting Group |
Watch Williams' presentation. |
| March 17, 2016 | "Audits Got You Down? Be Prepared! Let’s Talk About Quality Management in Research" Julie Doherty, Director, Office of Academic Affairs, Human Research Protections Office |
Watch Doherty's presentation. Download the checklist. |
| February 18, 2016 | "Non-Human Subjects, Exempt, and Expedited Research: What YOU Need to Know" Tara Catanzariti, IRB Administrator, Human Research Protections Office |
Watch Catanzariti's presentation. |