| Date |
Topic/Speaker |
|
March 2026
|
What To Do When Everything Goes Wrong
Laura Mowers, MS, CCRP
IRB Specialist at Trinity Health New York
|
|
February 2026
|
The Importance of Mentorship in Clinical Research
Anthony Keyes, MBA, PMP
Assistant Director, Clinical Workforce Operations
Johns Hopkins University, Institute for Clinical and Translational Research
|
|
January 2026
|
Clinical Research Best Practices: Regulatory Binder
Javier Rosales, M.S., ACSM EP-C
Clinical Research Specialist
Department of Pain and Translational Symptom Science
University of Maryland School of Nursing
|
|
November 2025
|
The How Can I Help "Chore" List: Learning Through the Lens of a Clinical Research Specialist
Carin Clingan, MS, CNS, LDN
Senior Clinical Research Assistant
Department of Pain and Translational Symptom Science
University of Maryland School of Nursing
|
|
October 2025
|
Through the Family Lens: Using Photovoice to Understand Family Communication in Serious Pediatric Illness
Kim Mooney-Doyle, PhD, RN, CPNP-AC, FAAN
Associate Professor
Department of Family and Community Health
University of Maryland School of Nursing
Associate Member, Program in Population Science
University of Maryland
Marlene and Stewart Greenebaum Comprehensive Cancer Center
|
|
September 2025
|
Survey Research Methods: Question Development and Validation
Jessica Pelletier Brown, PhD
Associate Professor
Department of Epidemiology and Public Health
University of Maryland School of Medicine
Director, Clinical and Translational Research Informatics Center
|
|
August 2025
|
Noncompliance or Research Misconduct? Definitions and Policies for Researchers
Kaylin A. Adipietro, PhD, Research Integrity Specialist, Office of Accountability and Compliance, UMB
Stephan Vigues, PhD, Research Integrity Officer, Director, Research Integrity Office, UMB
Bruce K. Krueger, PhD, Professor of Pharmacology and Physiology and of Psychiatry, UMSOM, Research Ombuds, UMB
|
|
June 2025
|
The UMB Investigator Manual: Key Points and Considerations
Casey Jackson MS, CCRP
|
|
May 2025
|
Internal Quality Control: A Guide to Checking Your Work
Thea Nash, MSHS, CCRP
Quality Assurance and Compliance Director
Clinical Research Management Office
Greenebaum Comprehensive Cancer Center
|
|
April 2025
|
Why Patient-Centered Research Practices Are Worth It
Cindy Baez, BA
Clinical Research Technical Assistant
UMB School of Social Work
|
|
March 2025
|
Veeva SiteVault Electronic Regulatory Binder
Casey Jackson, MS, CCRP
Sophie Harper, MS, CCRP
Aly Kwon, MS, CCRC, ACRP-PM
|
|
February 2025
|
Demystifying Data Agreements at UMB
Casey Jackson, MS, CCRP
|
|
January 2025
|
Joint UMSON and Baltimore SOCRA Chapter Meeting: “Roles and Responsibilities of Sponsors and Investigators”
Donna Headlee, BSN, RN, CCRP
|
|
November 2024
|
A Regulatory Binder QA Journey
Casey Jackson, MS, CCRP
|
|
October 2024
|
Scary Compliance
Multiple Local and National Surprise Speakers!
|
|
September 2024
|
Informed Consent Approaches In Human Subjects Research
Casey Jackson, MS, CCRP
|
|
August 2024
|
The Changing Ethics of Informed Consent and Biospecimens in Clinical Research
Casey Snoddy, BS, CCRP
|
|
June 2024
|
Exemption and Risk Determination in Human Research Using Devices
Donna Headlee, RN, BSN, CCRP
|
|
May 2024
|
The Voice of the Research Participant
Jeffrey Wells
Patient and Research Participant
|
|
March 2024
|
Joint UMSON MRS and Baltimore SOCRA Chapter Meeting: SOP on SOPs
Aryn Knight, BS, CCRP
Associate Vice President
Clinical Research Memorial Hermann Health System
|
|
February 2024
|
Community-Based Participatory Research in Action: Lessons Learned from an Academic-Community Collaboration
Doris Titus-Glover, PhD, RN
Assistant Professor
University of Maryland School of Nursing
|
|
January 2024
|
"Navigating the “IRB” When You're Not Doing Research"
Casey Jackson, MS, CCRP
Director, Research Quality and Compliance
University of Maryland School of Nursing
|
|
November 2023
|
"Pragmatic Clinical Trials: Research in the 'Real-World'”
Joan Carpenter, PhD, CRNP, ACHPN, FPCN
Assistant Professor
University of Maryland School of Nursing
|
|
October
2023
|
"Navigating the Single IRB Process"
Nichelle Cobb, PhD
Senior Advisor for Strategic Initiatives
Association for the Accreditation of Human Research Protection Programs
Michael Linke, PhD, CIP
SMART IRB Program Director for Education and Training; Chair, University of Cincinnati IRB and StrokeNet Central IRB; Adjunct Professor of Internal Medicine
University of Cincinnati
Polly Goodman, CIP
Associate Director, Regulatory Affairs Operations for SMART IRB
Harvard Catalyst
|
| September 2023 |
"Research Integrity and Scientific Misconduct"
Kaylin A. Adipietro, PhD
Research Integrity Specialist
Office of Accountability and Compliance
University of Maryland, Baltimore
|
| August 2023 |
“Research Participant Payment Considerations”
James Campbell, MD, MS
Professor, Department of Pediatrics
University of Maryland School of Medicine
Center for Vaccine Development and Global Health
|
| June 2023 |
"Research Record Retention & Destruction: Tips and Best Practices"
Casey Jackson, MS, CCRP
Research Quality Manager
University of Maryland School of Nursing
Gyasi Moscou-Jackson, PhD, MHS, RN
Nurse Scientist
University of Maryland Medical Center
|
| 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
|
| 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
|
| February 2023 |
"FERPA and Research"
Stephanie Suerth, MPA, CCEP
Acting Title IX Coordinator
Director, Special Projects
University of Maryland, Baltimore
Julie Doherty, DM, MSN, RN, CIP, CCEP
Assistant Vice President, Research Compliance
Office of Accountability & Compliance
University of Maryland, Baltimore
|
| January 2022 |
"NIH Data Sharing Policy"
Taunton Paine, MA Director, Scientific Data Sharing Policy Division
Office of Science Policy
National Institutes of Health
|
| November 2022 |
"Smart IRB Process and External IRB Reliance at UMB"
Julie Doherty DM, MSN, RN, CIP, CCEP
Assistant Vice President, Research Compliance
Office of Accountability & Compliance
University of Maryland, Baltimore
|
October
2022 |
"HIPPA Security and Privacy of Data, with a Special Focus on Research"
Peter Murray, PhD, CAS, MS
Senior Vice President for Information Technology and CIO
University of Maryland, Baltimore
|
| September 2022 |
"Storytelling in Research"
David O. Fakunle, PhD
Associate Faculty
Johns Hopkins Bloomberg School of Public Health
|
| August 2022 |
"Online Research Best Practices"
Christina L. Wright, MA, CIP
IRB Exempt/Expedited Team Lead
Virginia Commonwealth University
Chiara Acquati, PhD, LMSW
Assistant Professor
University of Houston Graduate College of Social Work
|
| June 2022 |
"Qualitative Research and the IRB: A Primer for Researchers"
Patricia Condon, PhD
Research Data Services Librarian
University of New Hampshire
Andrew Hedrick, MPA, CIP
Senior IRB Protocol Analyst
The Ohio State University
|
| May 2022 |
"Community Based Participatory Research: Challenges and Rewards"
Julie Doherty, DM, MSN
Assistant Vice President
Research Compliance
Robert E. Rosenthal, MD
IRB Chair and Professor
University of Maryland School of Medicine
|
| April 2022 |
"Research Consent Part 7: Electronic consent - what is it and what is it not?"
Casey Jackson, MS, CCRP
Research Quality Manager
University of Maryland School of Nursing
|
| March 2022 |
"Research Consent Part 6: Regulatory & Ethical Considerations (Vulnerable Populations, assents, and short form consents)"
Jon Mark Hirshon, MD, MPH, PhD
Professor, Department of Emergency Medicine
Senior Vice-Chairman, IRB
University of Maryland, Baltimore
|
| February 2022 |
"Research Consent Part 5: Informed Consent in Human Subjects Research: Untangling Consent Waivers"
Casey Jackson MS, CCRP
Research Quality Manager
University of Maryland School of Nursing
|
| January 2022 |
"Clinicaltrials.gov: All you need to know"
Anthony Keyes, MBA, PMP
Program Administrator
Johns Hopkins University School of Medicine
|
| November 2021 |
"Research Consent Part 4: Informed Consent in Human Subjects Research: Tips and Guidance on Consent Writing at UMB"
Casey Jackson, MS, CCRP
Research Quality Manager
University of Maryland School of Nursing
|
| October 2021 |
"Research Consent Part 3: Integrating Health Literacy into the Informed Consent Process: Tips for Developing Understandable Consent Materials"
Sylvia Baedorf Kassis, MPH
Program Manager
Multi-Regional Clinical Trials Center of Brigham and Women’s Hospital and Harvard
Christopher Trudeau, JD
Associate Professor of Law
University of Arkansas at Little Rock, William H. Bowen School of Law
|
| September 2021 |
"Why should we care about protecting human research participates and how can we do it well?"
Marianna Azar
Program Specialist, Division of Education and Development
Office for Human Research Protection
U.S. Department of Health and Human Services
|
| August 2021 |
"Research Consent Part 2: Required Elements of Consent"
Jan Martinez, MS, CIP, CLSSGB
IRB Manager
Human Research Protections Office
University of Maryland, Baltimore
Casey Jackson MS, CCRP
Research Quality Manager
Office of Research and Scholarship
University of Maryland School of Nursing
|
| June 2021 |
"Research Consent Part 1: History, Application, and Process"
Jan Martinez, MS, CIP, CLSSGB
IRB manager
Human Research Protections Office
University of Maryland, Baltimore
Casey Jackson, MS, CCRP
Research Quality Manager
Office of Research and Scholarship
University of Maryland School of Nursing
|
| May 2021 |
"Site and Staff Engagement: Resources and Guidance for Understanding Who is Engaged in Your Human Subjects Research Protocol"
Casey Jackson, MS, CCRP
Research Quality Manager
Office of Research and Scholarship
University of Maryland School of Nursing
|
| April 2021 |
"DocuSign Use for Research Compliant e-Signature Capture"
Douglas Bowser
Executive Director, Administrative and Academic Systems
Center for Information Technology Services (CITS)
University of Maryland, Baltimore
Eunissa Yancy
IT Senior Specialist
Center for Information Technology Services (CITS)
University of Maryland, Baltimore
|
| March 2021 |
"Reportable New Information (RNI) - What UMB Researchers NEED to Know"
Julie Doherty, DM, MSN, RN, CIP, CCEP
Executive Director, Research Protections
Human Research Protections Office
University of Maryland, Baltimore
|
| February 2021 |
"Auditing Human Subject Research"
LaToya Lewis, MS, MT (ASCP), CCRP, CCEP
Compliance Specialist
Office of Accountability and Compliance
University of Maryland, Baltimore
|
| January 2021 |
“Pediatric Research”
James D. Campbell, MD, MS
Professor of Pediatrics and IRB Vice Chair
University of Maryland School of Medicine
|
| October 2020 |
"QI vs. Research"
Casey Jackson, MS, CCRP
Research Quality Manager
Office of Research and Scholarship
University of Maryland School of Nursing
|
| September 2020 |
"Conflicts of Interest in Research"
Alison J. Watkins, JD, MS
AVP Enterprise Risk & Policy Oversight
Conflict of Interest Officer
University of Maryland, Baltimore
|
| August 2020 |
"Is my study exempt? Understanding exemption criteria"
Jessica Rowe, MA, MS, CCRP
Human Research Protection Program Manager
Emig Research Center WellSpan Health
|
| June 2020 |
"Applying the 10th Principle of Good Clinical Practice (GCP): Good Data and Record Management Practices"
Casey Jackson, MS, CCRP
Research Quality Manager
Office of Research and Scholarship
University of Maryland School of Nursing
|
| May 2020 |
"Non-Human Subjects Research Determinations"
Maria Drayton, BS
IRB Analyst
Human Research Protections Office
University of Maryland, Baltimore
|
| April 2020 |
"Best Practices for Research Data Management"
Jean-Paul Courneya
Library Research Info Specialist
Health Sciences and Human Services Library
University of Maryland, Baltimore
Amy Yarnell
Data Services Librarian
Health Sciences and Human Services Library
University of Maryland, Baltimore
|
| Feb. 2020 |
"Lean Six Sigma in Research: Process Improvement, Minimizing Waste, CAPAs, and More"
Emma Barkman, MHA, CCRP
Greenebaum Comprehensive Cancer Center
|
| Jan. 2020 |
"HIPAA Awareness"
Kent Buckingham
Executive Director
Office of Information Technology and Facilities Management
HIPAA & IT Security Officer
University of Maryland School of Dentistry
|
| Nov. 2019 |
"Preventing and Investigating Research Misconduct"
Stephan Vigues, PhD
Program Director, Research Accountability and Compliance Monitoring
University of Maryland, Baltimore
|
| Oct. 17, 2019 |
"Conducting Research with Pediatric Populations"
James D. Campbell, MD, MS
Professor of Pediatrics and IRB Vice Chair
University of Maryland School of Medicine
|
| Sept. 19, 2019 |
"Developing Better Consent Forms"
Everly Brown, MLIS
Head of Information Services
Health Sciences and Human Services Library
University of Maryland, Baltimore
Michele Nance, MS
Reference Associate
Health Sciences and Human Services Library
University of Maryland, Baltimore
|
| August 15, 2019 |
"Human Research Protections Program sIRB Processes & Workflow: Relying on an External IRB"
Julie Doherty, DM, MSN, RN, CIP, CCEP
Director, Human Protections Administrator/Human Research Protections Program
University of Maryland, Baltimore
|
| June 20, 2019 |
"Informed Consent and Ethical Considerations in Clinical Trials"
Jon Mark Hirshon, MD, MPH, PhD
Professor
Institutional Review Board Senior Vice Chair
University of Maryland School of Medicine
|
| May 16, 2019 |
"Conducting Research with Pediatric Populations"
James D. Campbell, MD, MS
Professor of Pediatrics and IRB Vice Chair
University of Maryland School of Medicine
|
| April 22, 2019 |
"Research Involving Participants with Diminished Capacity to Consent"
Leslie I. Katzel, MD, PhD
Associate Professor
Baltimore VA Medical Center
|
| March 28, 2019 |
"Applying the Revised Common Rule to Nursing Research"
Monique E. Tadeo, MS, CIP
Deputy Director, Research Protections Division
Department of the Navy
Human Research Protection Program
Office of Naval Research
Warfighter Performance Department
Jessica Rowe, MA, MS, CCRP
Research Quality Improvement Manager
University of Maryland School of Nursing
Office of Research and Scholarship
|
| Feb. 12, 2019 |
"Ensuring Institutional Compliance with Clinicaltrials.gov "
Antony Keyes, MBA, PMP
Aliya Lalji, MD
Johns Hopkins University School of Medicine |
| Jan. 17, 2019 |
"My Collaborator’s Keeper: When You Can Be Held Responsible for the Misconduct of Others"
Sarah N. Archibald, PhD, MS, MA, CCEP
Research Integrity Officer
Program Director, Research Integrity and Research Administration Certification Program
UMB Office of Accountability and Compliance
|
| Nov. 15, 2018 |
"Continuous Stakeholder Engagement in Research"
Hillary A. Edwards, MPH
Associate Director of Program Management and Evaluation
PATIENTS Program, PHSR
University of Maryland, School of Pharmacy
|
| Oct. 18, 2018 |
"Conducting VA research"
Frederick M. Ivey, PhD
Human and Animal Research Protections Officer
Baltimore Research and Development Service
VA Maryland Health Care System
|
| Sept. 20, 2018 |
"Quality Management in Behavior Research"
Jessica Rowe, MA, MS, CCRP
Research Quality Improvement Manager
University of Maryland School of Nursing
|
| Aug. 16, 2018 |
"Demystifying Expedited Event Reporting in Clinical Research"
Elizabeth (Liz) Ness, MS, BSN, RN
Director, Office of Education and Compliance
Center for Cancer Research
National Cancer Institute
|
| June 21, 2018 |
"FERPA and Research: The Other Privacy Law"
Stephanie Suerth
Education and Outreach Program Director
Office of Accountability and Compliance
|
| May 17, 2018 |
"Data Safety Monitoring in Human Subjects Research: Using Oversight to Avoid Oversights"
Frederick Luthardt
Manager, Compliance Monitoring Program
Johns Hopkins University School of Medicine
|
| April 19, 2018 |
"Navigating the Changing Regulatory Landscape- How the Common Rule Changes Will Impact You"
Madeleine Williams
Senior Consultant
Huron Consulting
|
| April 11, 2018 |
"Back to Basics: Informed Consent in Human Subjects Research"
Jessica Rowe, MA, MS, CCRP
Office of Research and Scholarship
University of Maryland School of Nursing
|
| March 15, 2018 |
"Protocol Development: A Practical Approach"
Kathleen Palmer, BSN, RN
Program Coordinator
University of Maryland School of Medicine
Program for Personalized and Genomic Medicine
|
| Feb. 15, 2018 |
"Quality in Good Clinical Practice"
Anita Moore, MS, RN, Nurse Consultant
Centers for Medicare & Medicaid Services
Quality, Safety, & Education Division |
| 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 |
| Oct. 19, 2017 |
"Ethics of Biobanking"
Robert Rosenthal, MD
Professor and Institutional Review Board Chair
University of Maryland, Baltimore |
| 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 |
| 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 |
| June 15, 2017 |
"Health Survey Research Methods"
Presented by Jessica Brown, PhD
Assistant Professor, University of Maryland School of Medicine |
| 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 |
| 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 |
| 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 |
| Feb. 16, 2017 |
"Considerations in Social Behavioral Research"
Seth Himelhoch, MD, MPH |
| 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 |
| Jan. 19, 2017 |
"Fostering Responsible Conduct of Research"
presented by Adil Shamoo, PhD
University of Maryland School of Medicine |
| Nov. 17, 2016 |
"UMB Research Integrity Office: What We Do and How We Do It"
Stephan Vigues, PhD
Accountability and Compliance, Research Integrity Office |
| Oct. 20, 2016 |
"Children in Clinical Research: Ethical and Regulatory Considerations in Pediatrics"
James Campbell, MD MS
University of Maryland School of Medicine |
| 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
|
| 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 |
| June 16, 2016 |
"What’s So Essential About Essential Documents? The Regulatory File"
Jessica Rowe, MA, MS, CCRP
UMSON Office of Research and Scholarship |
| May 12, 2016 |
"Clinical Research Data Management"
Elizabeth Ness, MS, RN
Center for Cancer Research |
| April 21, 2016 |
"Research Misconduct"
Sarah N. Archibald, PhD
Research Integrity Officer
University of Maryland, Baltimore |
| March 24, 2016 |
"Proposed Changes to the Common Rule: What Does it All Mean?"
Madeleine Williams, Huron Consulting Group |
| 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 |
| February 18, 2016 |
"Non-Human Subjects, Exempt, and Expedited Research: What YOU Need to Know"
Tara Catanzariti, IRB Administrator, Human Research Protections Office |