{"id":232,"date":"2010-01-13T11:44:20","date_gmt":"2010-01-13T16:44:20","guid":{"rendered":"https:\/\/www.bumc.bu.edu\/crro\/?page_id=232"},"modified":"2026-04-29T10:36:27","modified_gmt":"2026-04-29T14:36:27","slug":"past-seminars","status":"publish","type":"page","link":"https:\/\/www.bumc.bu.edu\/crro\/training-education\/past-seminars\/","title":{"rendered":"Seminar Library"},"content":{"rendered":"

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Date<\/strong><\/td>\nTitle and Presenter<\/b><\/td>\nMaterials<\/strong><\/td>\n<\/tr>\n
4\/22\/2026<\/td>\nInformed Consent Form Readability as Ethical Practice<\/span><\/strong><\/b>
\nStephanie Warth – Human Subjects Research Education Manager, CRRO<\/span><\/td>\n		Video
\nSlides<\/a><\/td>\n<\/tr>\n
3\/25\/2026<\/td>\nThe Importance of Protocol Adherence: Why it Sometimes Doesn’t Happen and How to Ensure it Does!<\/span><\/strong><\/b>
\nMary-Tara Roth, RN, MSN, MPH – Director, Clinical Research Resources Office<\/span><\/td>\n		Video
\nSlides<\/a><\/td>\n<\/tr>\n
2\/25\/2026<\/td>\nDon\u2019t Ghost Your Study: Proper Closeout for IRB and IT<\/span><\/strong><\/b>
\nCarolyn Swain, MPH, CIP – Senior IRB Analyst
\nDavid Corbett, JD – Infosec Compliance Manager & HIPPA Security<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
1\/21\/2026<\/td>\n\u00a0From K Aims to Execution: Building the Behavioral and Implementation Clinical Research Infrastructure as an Early Career Investigator<\/span><\/strong><\/b>
\nKirsten Austad, MD, MPH – Co-Director, Evans Center for Implementation & Improvement Science (CIS)
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
12\/17\/2025<\/td>\n\u00a0You Be the IRB: Case Studies in Human Research Protection<\/span><\/strong><\/b>
\nMatt Ogrodnik, MS, CIP-\u00a0 OHRA Director
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
10\/22\/2025<\/td>\n\u00a0Scooby Doo and Recruitment Too<\/span><\/strong><\/b>
\nKat Mott, BA \u2013 Senior IRB Analyst
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
9\/17\/2025<\/td>\n\u00a0INSPIR: Don\u2019t EXpire, Get INSPIRed<\/span><\/strong><\/b>
\nLin Themelis, MA, CIP \u2013 IRB Administrator
\nMark Testerman, MBA, CIP \u2013 Senior IRB Analyst II
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
6\/11\/2025<\/td>\n\u00a0De-Identification of Data: Helpful HIPAA for Investigators<\/span><\/strong><\/b>
\n<\/span>Patricia Bass \u2013 Associate General Counsel, BMC
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
5\/28\/2025<\/td>\n\u00a0From Collection to Collaboration: Making the Most of Repositories and Retained Samples<\/span><\/strong><\/b>
\n<\/span>Jamie Merrill, MPH, CIP \u2013 IRB Director, BMC\/BUMC
\n<\/span>Elizabeth Duffy, MA \u2013 Director, Laboratory and Biorepository Research Services Core, BMC<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
3\/12\/2025<\/td>\nAn Introduction to BMC\u2019s New Clinical Research Unit<\/span><\/strong><\/b>
\nRyan Schroeder – Director of Business Operations, Clinical Research Network and Clinical Research Unit, BMC
\nAnh Tran, MS – CRU Clinical Director, BMC<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
2\/12\/2025<\/td>\nBeyond Industry Trials: Clinical Research Billing and Finance in Awards and \u201cUnfunded\u201d Studies<\/strong><\/b>
\nMike Porreca, Director, Clinical Trial Office, BMC
\nSandy Lok, Contract Specialist, Research Contracting, BMC
\nKaye Mottola, CHRC, CPC, Research Policy and Education Manager, BMC<\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
1\/8\/2025<\/td>\nDisclosing Financial Conflicts of Interest in Research at BU & BMC
\n<\/b>Cassie Williams, MPH, Program Manager
\nJackie Presedo, CHRC, Research Compliance Manager<\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
12\/11\/2024<\/td>\nNon-Commercial IRB Cede Review and You: Policies, Processes, Tips, and Tricks
\n<\/b>Matt Orgodnik, MS, CIP – Director, Office of Human Research Affairs<\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
11\/20\/2024<\/td>\nSharing Research Results with Study Participants and Partners: Examples from the HEALing Communities Study
\n<\/b>Carly Bridden, MA, MPH – Project Director
\n<\/b><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
10\/9\/2024<\/td>\nTools in the Consent Backpack: Unpacking how to include participants with limited English proficiency
\n<\/b>Carolyn Swain, MPH, CIP \u2013\u00a0Senior IRB Analyst
\n<\/b><\/td>\n		Video<\/a>
\nSlides<\/a>
\n<\/a><\/td>\n<\/tr>\n
9\/18\/2024<\/td>\nRecent Changes to ClinicalTrials.gov: What every PI and Research Team Member Should Know
\n<\/span><\/span><\/strong><\/b>Karla Damus,\u00a0<\/span>PhD, MSPH, MN, RN FAAN \u2013\u00a0<\/span>Administrator, ClinicalTrials.gov and MCSR Research Licensure<\/span><\/td>\n		Video<\/a>
\nSlides<\/a>
\n<\/a><\/td>\n<\/tr>\n
5\/8\/2024<\/td>\nCommon Quality Assurance Review Findings: Lessons for Improving Your Own Research
\n<\/span><\/span><\/strong><\/b>Alyssa Pingitore, BS \u2013 Human Research Quality Manager, Office of Human Research Affairs, BUMC<\/span><\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
4\/10\/2024<\/td>\nScreening-Dooby-Doo: Unmasking Screening Best Practices
\n<\/span><\/span><\/strong><\/b>Jamie Merrill, MPH, CIP \u2014 BMC\/BUMC IRB Director<\/span>
\n<\/span>Katherine Mott, BA \u2013 BMC\/BUMC IRB Analyst<\/span>
\n<\/span><\/span><\/strong><\/b><\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
3\/13\/2024<\/td>\nClinical Research Billing II: Operational Process and Management
\n<\/span><\/span><\/strong><\/b>Kaye Mottola, MA, CPC, CHRC \u2013 Manager, Research Education, Research Operations, Boston Medical Center
\nMike Porreca \u2013 Senior Manager, Clinical Trials Office, Boston Medical Center<\/span>
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
2\/14\/2024<\/td>\nClinical Research Billing I: The Most Basic Basics
\n<\/span><\/span><\/strong><\/b>Kaye Mottola, MA, CPC, CHRC \u2013 Manager, Research Education, Research Operations, Boston Medical Center
\nMike Porreca \u2013 Senior Manager, Clinical Trials Office, Boston Medical Center<\/span>
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
1\/10\/2024<\/td>\nLanguage Diversity in Research – Resources & Tips
\n<\/span><\/span><\/strong><\/b>Ryan Schroeder, CRN Director
\nJohanna Chesley, Sr. Director CCRA
\nDuncan Schulte, CRN Regulatory Project Manager
\nQuinneil Simmons, CRN Program Manager
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
12\/13\/2023<\/td>\nReporting Adverse Events, Serious Adverse Events, and Unanticipated problems
\n<\/span><\/span><\/strong><\/b>Eric Devine, PhD: D<\/span>irector of the Clinical Studies Unit in the Department of Psychiatry and Vice-Chair for the BMC\/BUMC IRB<\/span>
\n<\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
11\/8\/2023<\/td>\nI have SOPs and know how to use \u2018em!
\n<\/span><\/span><\/strong><\/b>Mary-Tara Roth RN, MSN, MPH: Director of Clinical Research Resources Office<\/em><\/span>
\n<\/span><\/span><\/strong><\/b>Ryan Schroeder: Director of Clinical Research Network at BMC
\nDuncan Schulte: Regulatory Project Manager for Clinical Research Network at BMC<\/em><\/span><\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
10\/11\/2023<\/td>\nI Have Ceded Review \u2013 Now What to Do?
\n<\/strong><\/b>Matthew Ogrodnik, MS, CIP, Director, Office of Human Research Affairs<\/em>
\n<\/strong><\/b><\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
9\/13\/2023<\/td>\nConsents: The Good, The Hard, The Beautiful
\n<\/b>Rana Leed, MPH: Human Research Education Manager
\nRyan Schroeder: Director of Clinical Research Network at BMC<\/em><\/i>
\n<\/b><\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
6\/14\/2023<\/td>\nInstitutional Support and Resources for Human Subjects Research: Lightning Talks<\/b>
\nCTO<\/a>,\u00a0<\/span>IRB<\/a>,\u00a0<\/span>GCRU<\/a>,\u00a0<\/span>CRN<\/a>,\u00a0<\/span>IPS<\/a>,\u00a0<\/span>CDW<\/a>,<\/span>\u00a0<\/span>clinicaltrials.gov submissions<\/a>, CRRO<\/a><\/span><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
5\/10\/2023<\/td>\nHow to Win Friends\u00a0<\/span>(at the IRB)<\/em>\u00a0<\/span>and Influence People\u00a0<\/span>(to join your research study)<\/em><\/b>
\nLin Themelis, MA, MS, CIP \u2013 IRB Administrator<\/em>
\nJamie Merrill, MPH, CIP \u2014 BMC\/BUMC IRB Director<\/em><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
4\/12\/2023<\/td>\nOverview and Significance of Quality Assurance Process: You\u2019ve been selected for a routine QA Review \u2013 Now what?<\/b>
\nEmily Crowley, MPH, CIP \u2013 Human Research Quality Manager, Office of Human Research Affairs<\/em>
\nAlyssa Pingitore, BS \u2013 Human Research Quality Manager, Office of Human Research Affairs<\/em><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
3\/8\/2023<\/td>\nQuality Management: Taking a Proactive Approach and Using Self-Assessments to Ensure High Quality Research<\/strong>
\nRana Leed, MPH, Human Research Education Manager
\n<\/i>Mary-Tara Roth RN, MSN, MPH: Director of Clinical Research Resources Office<\/em><\/td>\n		Video<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
2\/8\/2023<\/td>\nStudy Startup and Initiation: The Agony and the Ecstasy<\/strong>
\nRana Leed, MPH, Human Research Education Manager<\/i><\/td>\n		Video\u00a0<\/a>
\nSlides<\/a><\/td>\n<\/tr>\n
1\/11\/2023<\/td>\nTranslational informatics tools to support health services and equity research at BMC and BU<\/strong>
\nWilliam G. (Bill) Adams, MD, Professor of Pediatrics and Informatics Director<\/i><\/sarah><\/em>
\nSarah Gasman, Senior Research Data Analyst, Data 4 Equity<\/em><\/td>\n		Video<\/a><\/p>\n

Slides<\/a><\/td>\n<\/tr>\n

12\/15\/2022<\/td>\nEngagement or Non-Engagement? That is the IRB Oversight Question<\/b>
\nMatthew Ogrodnik, MS, CIP, Director, Office of Human Research Affairs<\/em>
\nJamie Merrill, MPH CIP, Director Institutional Review Board<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
11\/2\/2022<\/td>\nBMC Clinical Research Standard Operating Procedures Implementation<\/strong>
\nMary-Tara Roth RN, MSN, MPH: Director of Clinical Research Resources Office<\/em>
\nRyan Schroeder: Director of Clinical Research Network at BMC<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
10\/19\/2022<\/td>\nREDCap: Case Studies<\/strong>
\nSarah Bredy, BA: Research Assistant in General Internal Medicine<\/em>
\nSarah Weber, MPH: Project Management Specialist in Infectious Disease<\/em>
\nKayla Brown, MS, MS: Psychiatry<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
9\/14\/2022<\/td>\nREDCap Basics
\n<\/strong>Tasha Coughlin, REDCap Administrator<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
6\/8\/2022<\/td>\nUsing Clinical Data Warehouse for Research: Real-World Case Studies in Data Literacy
\n<\/strong>Melissa Hofman, MSIS, Research Informatics Director, CDW for Research; Heather Hsu, Scientific Director, CDW for Research<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
5\/11\/2022<\/td>\nThe BMC\u00a0 Clinical Data Warehouse (CDW) for Research: Get Research-Ready Data for your\u00a0 Studies
\n<\/strong>Erin Ashe, MPH, Program Director, CDW for Research<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
4\/12\/2022<\/td>\nTo IRB or Not to IRB: That is the Question
\n<\/strong>Nicholas Cordella, MD, MSc, Medical Director, Quality & Patient Safety, BMC; Emily Jansen, MPH, Senior Program Manager, Quality & Performance Improvement for the QI Hub & Barry M. Manuel Continuing Medical Education Office; Brandon Finn, BA, IRB Analyst, BMC\/BUMC IRB; Jasmine Huerta, MD, MS, MPA, Internist, QI Fellow, BMC<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
3\/16\/2022<\/td>\nApplying Health Literacy to Clinical Research Communications
\n<\/strong>Sylvia Baedorf Kassis, MPH, Program Manager, Multi-Regional Clinical Trials Center, Brigham and Women’s Hospital and Harvard University<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
2\/9\/2022<\/td>\nConducting Research with Boston HealthNet Community Health Centers
\n<\/strong>Allyson Richmond, Program Manager, Boston HealthNet at Boston Medical Center; Matthew Ogrodnik, MS, CIP, Director, Office of Human Research Affairs<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/a><\/td>\n<\/tr>\n
1\/12\/2022<\/td>\nClinical Research Operations at Boston Medical Center: A guide to how the Clinical Trial Office can support successful, inclusive research practices
\n<\/strong>Johanna C. Chesley, MPH, Senior Director, Clinical Trials Office<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
12\/15\/2021<\/td>\nUpdate on Informatics Resources and Services for the BMC\/BUMC Community
\n<\/strong>Bill Adams, MD, Professor, BU School of Medicine<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
11\/17\/2021<\/td>\nCase Report Form Design
\n<\/strong>Kimberly Ann Dukes, PhD, Executive Director, Biostatistics and Epidemiology Data Analytics Center, BU SPH<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
10\/13\/2021<\/td>\n A Surfeit of Surveys: Exempt Category 2<\/strong>
\nDaly Franco, Senior IRB Analyst; Lin Themelis, IRB Administrator<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
9\/22\/2021<\/td>\nIRB Submission Overview for Chart Reviews & Secondary Analyses
\n<\/strong>Carolyn Swain, MPH, IRB\u00a0 Analyst; Emily Crowley, MPH, IRB Administrator<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
6\/9\/2021<\/td>\nResearch Repositories: What\u2019s new?\u00a0 Overview, Operations, and IRB submissions
\n<\/strong>Matthew Ogrodnik, MS CIP<\/em>, <\/strong>Director, Office of Human Research Affairs<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
5\/19\/2021<\/td>\nThe Story of ClinicalTrials.gov: Promoting Transparency and Scientific Integrity in Research<\/b>
\n<\/strong>Karla Damus, PhD, MSPH, RN, Administrator, ClinicalTrials.gov<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
4\/14\/2021<\/td>\nExperiences with an Investigator-Initiated Clinical Trial During COVID-19: Transitioning from Single- to Multi-center
\n<\/strong>Nicholas A. Bosch, MD, MSc, Assistant Professor of Medicine, BUSM<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
3\/17\/21<\/td>\nEducating our research community: Implicit and Explicit Bias in Research<\/strong>
\nMegan H. Bair-Merritt, MD, MSCE, Professor of Pediatrics, BUSM; Executive Director, Center for the Urban Child & Healthy Family, BMC<\/em><\/td>\n		Slides<\/a>
\nArticle<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
2\/10\/21<\/td>\nEthical Considerations for Social Media<\/strong>
\nKimberly Nelson, PHD, MPH, Assistant Professor of Community Health Sciences, BU SPH<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
1\/13\/21<\/td>\nAnything Goes?: What are the limits to research without consent in a “learning healthcare system”?
\n<\/strong>James Feldman, MD and Allan Walkey, MD<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
12\/16\/20<\/td>\nRemote and E-consent (including REDCap)
\n<\/strong>Mary-Tara Roth, RN, MSN, MPH, Director, Clinical Research Resources Office; Jung Lee, BS, Human Research Quality Manager; Emily Crowley, MPH, CIP, Senior IRB Analyst II<\/em>
\n<\/strong><\/td>\n		Slides 1<\/a>
\nSlides 2<\/a>
\nSlides 3<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
11\/18\/20<\/td>\n3 Case Studies on Implementation of REDCap in Clinical Research Studies
\n<\/strong>\u2013 Hira Shrestha, MA, Clinical Research Manager, NAS, Dept. of Pediatrics, Boston Medical Center<\/em>
\n\u2013 Sarah Weber, Research Study Coordinator, Section of Infectious Diseases, Boston Medical Center<\/em>
\n\u2013 Elizabeth Ragan, MPH, Administrative Manager, Section of Infectious Diseases, Boston Medical Center<\/em>
\n\u2013 Michael A. Garcia, MD, Pulmonary and Critical Care Medicine Fellow, Boston University\/Boston Medical Center<\/em>
\n\u2013 Nicholas A. Bosch, MD, MSc, Assistant Professor of Medicine, Pulmonary, Allergy, Sleep & Critical Care Medicine, Boston University School of Medicine<\/em><\/td>\n		Slides 1<\/a>
\nSlides 2<\/a>
\nSlides 3<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
10\/14\/20<\/td>\nThe Basics of Using REDCap for Study Data Collection
\n<\/strong>Tasha Coughlin, Research & Instructional Applications Manager, BUMC IT-EdMedia<\/em>
\n<\/strong><\/td>\n		Slides<\/a><\/p>\n

Video not available.<\/td>\n<\/tr>\n

9\/16\/20<\/td>\nCede Review and You — How to Navigate this Evolving “New World” of IRB Review
\n<\/strong>Matthew Ogrodnik, MS, CIP, IRB Director<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
6\/10\/20<\/td>\nResearch Privacy and Data Security
\n<\/strong>David Corbett, Scott Pasquino, Erika Barber<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
5\/27\/20<\/td>\nRecruitment Promotional Materials: Information and Training on New Process
\n<\/strong>Lillian Vautour, Adam Knee, and Josh Read,<\/em>
\nBMC Communications and Marketing<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
3\/11\/20<\/td>\nSurvey Design and Development for Researchers
\n<\/strong>Eliza Hallett, Department of Pediatrics<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
2\/12\/20<\/td>\nAsking the Right Question: Qualitative Research Design and Analysis
\n<\/strong>Jennifer Sikov, Department of Psychiatry<\/em><\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
1\/8\/20<\/td>\nClinical Adjudication Committees: Best Practices for Use in a Range of Study Designs
\n<\/strong>Jennifer Rooney, Section of Infectious Diseases<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
12\/11\/19<\/td>\nA Primer on the Regulatory Binder: How to Set up and Maintain Regulatory Documentation to Meet the Needs of Your Research
\n<\/strong>Mary-Tara Roth, Clinical Research Resources Office<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
11\/13\/19<\/td>\nGuidance for Research Teams when Onboarding New Research Staff
\n<\/strong>Claire Oppenheim, MPH, BMC Immigrant Health Center<\/i><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
10\/9\/19<\/td>\nData Do’s and Don’ts: Best Practices and Mistakes to Avoid
\n<\/strong>Fanny Ennever, PhD, BMC Research Compliance Officer<\/i><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
9\/11\/2019<\/td>\nBoston Medical Center Clinical Trials Office’s Short- and Long-Term Goals
\n<\/strong>Johanna Chesley and Mike Porreca, BMC Clinical Trials Office<\/i><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
6\/12\/2019<\/td>\nA Spectrum of Mixed Methods Research Designs<\/strong>
\nNellie Shippen, MA, <\/i>Research Coordinator,\u00a0<\/i>Department of Psychiatry<\/i><\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
5\/8\/2019<\/td>\nAvoiding and Responding to the Most Common IRB Application\u00a0Stipulations<\/strong>
\nLin Themelis, BA, MA, CIP, <\/em>IRB Administrator; Jamie Merrill, MPH, CIP, IRB Administrator;\u00a0<\/em>Kathryn Jones, BA CIP<\/em>, Senior IRB Analyst II;\u00a0<\/em>Emily Crowley, BS, MPH<\/em>, Senior IRB\u00a0 Analyst<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
3\/13\/2019<\/td>\nHow to Determine Withdrawal of Assent in an Inner-city Pediatric Population<\/strong>
\nGeorge O’Connor, MD,\u00a0 Professor of Medicine, Director, Adult Asthma Program;\u00a0<\/em>Lisa Gagalis, RN BSN, Clinical Project Manager RACR2, MUPPITS2, URECA, and CREW<\/em><\/o:p> <\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
2\/13\/2019<\/td>\nLessons Learned and Common Findings from QA Audits of Research Studies
\n<\/strong>Fiona Rice, MPH<\/i>, Human Research Quality Manager, OHRA;
\n<\/em>Gina Daniels, BS<\/i>, <\/em>Human Research Quality Manager, OHRA <\/em><\/o:p><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
1\/9\/2019<\/td>\nCeding Review and SMART IRB\u00a0\u00a0<\/strong>
\n\u00a0Matthew Ogrodnik, MS CIP, Director, BUMC\/BMC IRB<\/em><\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
12\/12\/2018<\/td>\nWhat You Need to Know About\u00a0HIPAA and Data Security\u00a0for Research<\/strong>
\nSean Nabi, JD, CIPP\/US, Privacy Officer, BMC; Diane Lindquist, JD, Director Health Privacy and Compliance, BU;\u00a0David Corbett, JD, BBA, Security Officer, BUMC; Matt Ogrodnik, MS CIP, Director, BUMC\/BMC IRB<\/em><\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
11\/7\/2018<\/td>\nInequities in Clinical Research: How study teams can support Black participants<\/strong>
\nJonathan Jackson, PhD, Director, Community Access, Recruitment and Engagement, <\/em>
\nCARE Research Center, MGH Research Institute<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
10\/10\/2018<\/td>\nKeeping Research Transparent and Unbiased by Managing Potential Conflicts of Interest (COI)<\/strong>
\nFanny Ennever, PhD CIP, <\/em>BMC Research Compliance Officer; David Coleman, MD, Chair, COI Committee, Professor & Chair, <\/em>Dept of Medicine, BUSM; <\/em>Heather Skinner, JD,<\/em>\u00a0<\/strong><\/em>Assist Director, Research Integrity COI\/EC, BU<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
9\/12\/2018<\/td>\nImportant\u00a0Updates about the\u00a0OHRA, IRB, CRRO and\u00a0RPN, and\u00a0the 2018\u00a0Common Rule
\n<\/em><\/strong>John Ennever, MD PhD CIP, <\/em>Director, Office of Human Research Affairs; Matt Ogrodnik, MS CIP, Director, BUMC\/BMC IRB;\u00a0<\/em>and\u00a0Mary-Tara Roth, RN MN MPH, Director, Clinical Research\u00a0and Resources Office<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
6\/13\/2018<\/td>\nDatabase and Survey Development for\u00a0 Clinical Research Studies<\/em><\/strong>
\nJoe Palmisano, Assist Director, BEDAC; Tasha Coughlin, Data Manager, BU CTSI; Linda Rosen, CDW Research Manager;\u00a0and\u00a0Howard Cabral, Director, Biostatistics and Research Design Program, BU CTSI<\/em><\/em><\/td>\n		Slides<\/a>
\nVideo<\/a> (partial recording)<\/td>\n<\/tr>\n
5\/9\/2018<\/td>\nThe Use of Large Data Sets to Respond to Policy Relevant Questions in Health Services Research<\/strong>
\nLewis E. Kazis, Sc.D., Professor of Health Policy and Management, Director, HOU, BUSPH<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
4\/24\/2018<\/td>\nNew Requirements for Registration, Updating and Results Reporting for ClinicalTrials.gov<\/strong>
\nKarla Damus, PhD MSPH MN RN, Administrator BMC\/BUMC ClnicalTrials.gov<\/em><\/td>\n		Slides<\/a>
\nNo video<\/td>\n<\/tr>\n
4\/11\/2018<\/td>\nHow to develop a Corrective and Preventative Action Plan (CAPA) that even the FDA will love<\/strong>
\nFiona Rice,<\/strong>\u00a0MPH, Human Research Quality Manager, OHRA; Mary-Tara Roth,\u00a0RN, MSN, MPH,\u00a0Director, CRRO<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
2\/14\/2018<\/td>\nCommon Statistical Issues in Biomedical Research Studies
\n<\/strong>Howard Cabral, PhD, MPH, Director, Biostatistics and Research Design Program, BU CTSI<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
1\/10\/2018<\/td>\nHIPAA and Research Data Security
\n<\/strong>Diane Lindquist, JD, Director Health Privacy & Compliance, BU;\u00a0<\/em>David Corbett, JD, BBA, Security Officer, BUMC\u00a0<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
12\/13\/2017<\/td>\nClinical Research Billing Compliance
\n<\/strong>Joyce Samet, JD, Research Compliance Officer, Boston Medical Center<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
11\/8\/2017<\/td>\nAdvice and Perspectives from the BMC\/BU Medical Campus IRB Panel Chairs
\n<\/strong>James Feldman, MD, MPH, (Chair, Panel Blue), Glenn Markenson, MD<\/em>
\n(Chair, Panel Green), Sanford Auerbach, MD (Chair, Panel Red), and David Kaufman, ScD (Chair, Panel Orange)<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
10\/11\/2017<\/td>\nWhen a Single IRB Reviews for Multiple Sites: The Complexities of “Simplification”
\n<\/strong>John F. Ennever, MD, PhD<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
9\/13\/2017<\/td>\nDIY IRB ABCs: Teaching You to Fish (and New Common Rule Changes)<\/em>
\n<\/strong>Fanny Ennever, PhD, CIP, Manager Regulatory Policy Development, OHRA<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
6\/21\/2017<\/td>\nUpdates on the RPN (Research Professionals Network)\u00a0<\/strong><\/td>\nSlides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
5\/10\/2017<\/td>\n\u00a0Investigational Pharmacy Service at BMC
\n<\/strong>Stephen Zalewski, PharmD, CCRC<\/em>
\n<\/strong><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
4\/12\/2017<\/td>\nResearch Data Security
\n<\/em><\/strong>Thomas Moore, MD, Associate Provost, Medical Campus, and Executive Director, Office of Human Research Affairs;\u00a0<\/em>David Corbett, JD,\u00a0BU Medical Campus Information Security Officer<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
3\/8\/2017<\/td>\nDigital Strategies for Recruitment and Retention<\/strong>
\nLisa Marceau, MPH, PMP;\u00a0 Julia Coleman, BA, PMP<\/em>
\nNew England Research Institutes<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
2\/8\/2017<\/td>\n\u00a0Decisional Capacity in Research Informed Consent
\n<\/strong>Robert Stern, PhD<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
1\/18\/2017<\/td>\nClinicalTrials.gov Compliance Issues
\n<\/strong>Joyce S. Samet, JD, Research Compliance Officer, Boston Medical Center; Karla Damus, PhD, MSPH, MN, RN<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
12\/14\/2016<\/td>\nLaunching the BMC\/BU Medical Campus Research Professionals Network (RPN)
\n<\/em><\/strong>Mary-Tara Roth, RN, MSN, MPH; Karla Damus, PhD, MSPH, MN, RN<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
11\/30\/2016<\/td>\nStrategies Used to Meet Recruitment Goals and Retain > 90% of Low Income Mothers<\/strong>
\n in a Year-Long RCT\u00a0 \u00a0<\/strong>Jenna Sandler, BS, MPH<\/em><\/td>\n		Slides<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
11\/9\/2016<\/td>\nClinical Research Billing and Related Compliance Issue
\n<\/strong>Joyce S. Samet, JD,\u00a0Research Compliance Officer, Boston Medical Center<\/em><\/td>\n		Video<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
10\/26\/2016<\/td>\nINSPIRing Changes to the IRB Process: New Templates and More
\n<\/strong>John F. Ennever, MD, PhD, CIP<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
9\/14\/2016<\/td>\nIRB Makeover: Top Ten Recent Changes
\n<\/strong>Fanny Ennever, PhD, CIP<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
6\/8\/2016<\/td>\nEquivalent Protections: Altered Requirements for Minimal Risk Research<\/strong>
\n<\/strong>Fanny Ennever, PhD, CIP<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
5\/19\/2016<\/td>\nMoving from Readability to Comprehension<\/strong>
\nMichael Paasche-Orlow, MD, MPH<\/em><\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
4\/13\/2016<\/td>\nSecrets of a No-Hassle Material Transfer Agreement (MTA)
\n<\/strong>Patricia Bass, JD<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
3\/9\/2016<\/td>\nGood Study Design and Analysis Plans as Features of Ethical Clinical Research<\/strong>
\nJanice Weinberg, ScD<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
2\/10\/2016<\/td>\nCriteria for IRB Approval and Case Studies in Pediatric Research
\n<\/strong>Carolyn Dunbar-Masterson, BSN, RN<\/td>\n		Slides<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
1\/27\/2016<\/td>\nRecent Changes in Oversight of Human Research at BU Medical Campus and BMC: <\/strong>What do they Mean for You?<\/strong>
\n<\/strong>Thomas J. Moore, MD;\u00a0Mary-Tara Roth, RN, MSN, MPH;\u00a0John Ennever, MD, PhD<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
12\/9\/2015<\/td>\nThe 111 Criteria: What it Takes to Get Your Study Approved<\/strong>
\nJohn Ennever, MD, PhD<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
11\/4\/2015<\/td>\nThe BMC Clinical Data Warehouse — Lots of Answers…What’s the Question?<\/strong>
\nLinda Rosen, MSEE<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
10\/14\/15<\/td>\nNew INSPIR Application Going LIVE on October 17th: Your Chance for a Sneak Peek!<\/strong>
\nJohn Ennever, MD, PhD<\/td>\n		Video<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
9\/30\/2015<\/td>\n Standard Operating Procesures (SOPs) in the Clinical Research Setting<\/strong>
\nMary-Tara Roth, RN, MSN, MPH<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
6\/10\/2015<\/td>\n Data and Safety Monitoring for Clinical Trials (DSMBs, DMCs): Principles, Operations, Personal Experiences<\/strong>
\nTheodore Colton, Sc.D.<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
5\/13\/2015<\/td>\nFirst Looks — The New INSPIR Application<\/strong>
\nJohn F. Ennever, MD, PhD<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
4\/8\/2015<\/td>\nThe Distinction of Quality Improvement (QI) Activities from Research: When is My Project Considered Research and What Steps Do I Take for IRB Review and Approval?<\/strong>
\nJames M. Moses, MD, MPH<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
3\/11\/2015<\/td>\nClinical Trials Registration Requirements: What You Should Know about ClinicalTrials.gov<\/strong>
\nEmily Ouellette, JD<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
2\/11\/2015<\/td>\n(Mis)conceptions about Therapeutic Misconception<\/strong>
\nSusan S. Fish, PharmD, MPH<\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
1\/14\/2015<\/td>\nChart Review FAQ’s: A Guide for Submission to the BUMC IRB
\n<\/strong>Matthew Ogrodnik, Senior IRB Analyst, BUMC<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
11\/18\/2014<\/td>\n Prisoner Data in Clinical Research: Identifying it, Protecting it, and Appropriately Using it<\/strong>
\nMary Buckley, MPH<\/td>\n		Slides<\/a>
\nVideo
\n<\/a> Podcast<\/a><\/td>\n<\/tr>\n
10\/22\/2014<\/td>\n Changes in the IRB Processes – Coming Now and in the Future
\n<\/strong>John Ennever, MD, PhD, and Staff of the IRB Office<\/td>\n		Slides<\/a>
\nVideo
\nPodcast<\/a><\/td>\n<\/tr>\n
9\/10\/2014<\/td>\nWhat Would You Do? (Put Your IRB Hat On!)
\n<\/strong> Mary-Tara Roth, RN, MSN, MPH Mary Banks, RN, BSN<\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
6\/25\/2014<\/td>\nIt Takes a Village: Leading a Complex Clinical Trial
\n<\/strong> Patty Mitchell, RN<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
5\/21\/2014<\/td>\nThe Basics of Adverse Event Monitoring and Reporting
\n<\/strong> Mary-Tara Roth, RN, MSN, MPH<\/td>\n		Slides<\/a>
\n<\/a> Video<\/a>
\nPodcast <\/a><\/td>\n<\/tr>\n
4\/16\/2014<\/td>\nProtecting Human Research Data: How to Make your Laptop, Tablet, and Smart Phone Secure…and bring your device to get it password protected and encrypted!
\n<\/strong> Thomas Moore, MD; Quinn R. Shamblin, CISM, CISSP, ITIL\/Former: PMP, GIAC GCFA; Sumit Sehgal, CISSP, CISA; Robert Sprinkle, MS<\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
3\/19\/2014<\/td>\n Is i2b2 for You? An Introduction to Health Outcome Monitoring and Research Using the BU-CTSI i2b2 Clinical Data System\u00a0 \u00a0\u00a0<\/strong>William G. Adams, MD<\/td>\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
2\/19\/2014<\/td>\n Processing and Negotiating Clinical Trial Agreements
\n<\/strong> Anne Clark, JD<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
1\/15\/2014<\/td>\n Using a Clinical Data Warehouse for Research: Key Considerations and Practical Resources at BMC and BUMC
\n<\/strong>Christopher Shanahan, MD, MPH, FACP<\/td>\n		 Podcast<\/a><\/td>\n<\/tr>\n
12\/11\/2013<\/td>\n Government Grant Opportunities Beyond the RO1: A Primer
\n<\/strong>Maura Harrington, MS<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
11\/25\/2013<\/td>\n Globalization of Clinical Trials: Stipulation and Perceptibility
\n<\/strong>Devon Parmar, MD, FCP (US)<\/td>\n		Slides<\/a>
\n<\/a> Video<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
10\/16\/2013<\/td>\nIdentifying, Assessing, and Resolving Issues in Social, Behavioral, and Educational Research (SBER)
\n<\/strong> Cynthia Monahan, MBA<\/td>\n		Slides<\/a>
\n<\/a> Video<\/a> Podcast<\/a><\/td>\n<\/tr>\n
9\/18\/2013<\/td>\nResearch Project Meeting Criteria for Exemption: Avoiding Common Pitfalls to Improve Prospects for Successful IRB Review!
\n<\/strong> Mary-Tara Roth, RN, MSN, MPH<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a> <\/a><\/td>\n<\/tr>\n
6\/19\/2013<\/td>\nData Management: Why You Should Care and What You Should Know<\/strong>
\nChristine E. Chaisson, MPH<\/td>\n		Slides<\/a>
\nVideo<\/a>
\nPodcast<\/a><\/td>\n<\/tr>\n
5\/15\/2013<\/td>\nCommon Statistical Issues in Biomedical Research<\/strong>
\nHoward Cabral, PhD, MPH<\/td>\n		Video<\/a>
\nPodcast<\/a>
\nSlides<\/a> <\/strong><\/td>\n<\/tr>\n
4\/12\/2013<\/td>\nEmergency Research and the Regs: Why Ignorance is not<\/em> Bliss
\n<\/strong>James Feldman, MD, MPH, FACEP, CIP<\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
3\/20\/2013<\/td>\nData and Tissue Repositories, Part 2<\/strong>
\nMary Banks, RN, BSN<\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
2\/20\/2013<\/td>\nData and Tissue Repositories, Part 1
\n<\/strong> Patricia A. Bass, JD, MPH<\/td>\n		Slides<\/a>
\n V<\/a>ideo<\/a><\/td>\n<\/tr>\n
1\/16\/2013<\/td>\nCommunity Based Participatory Research: Training Community Workers to Engage in Research
\n<\/strong> Brenda Heaton, PhD, MPH<\/td>\n		Slides<\/a>
\n<\/a> Video<\/a><\/td>\n<\/tr>\n
12\/19\/2012<\/td>\nChild Abuse Reporting Requirements in the Research Context
\n<\/strong>Robert Sege, MD, PhD<\/td>\n		Slides<\/a>
\n<\/a> Video<\/a><\/td>\n<\/tr>\n
11\/14\/2012<\/td>\nRecruiting Subjects: How the ReSPECT Registry and StudyFinder Can Help
\n<\/strong> Farrah Belizaire, BS; R. Joshua Reynolds, BM; Mary-Tara Roth, RN, MSN, MPH<\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
10\/17\/2012<\/td>\nThe BMC Clinical Data Warehouse: An Overview of the Possibilities for Research Using the Clinical Data Warehouse
\n<\/strong>Linda Rosen, MSEE<\/td>\n		Slides<\/a>
\nVideo<\/td>\n<\/tr>\n
9\/19\/2012<\/td>\nGetting Conflicts: An Overview of the Changes in Conflict of Interest Regulation and How It Affects Your Research
\n<\/strong> Jodi R. Edelstein, JD<\/td>\n		Slides<\/a>
\n Video<\/a><\/td>\n<\/tr>\n
6\/20\/2012<\/td>\nThe BUMC Research Occupational Health Program at BU\/BMC<\/strong>
\nThomas Winters, MD, FACOEM and Sandra Reno, RN<\/td>\n		No Slides
\nVideo<\/a><\/td>\n<\/tr>\n
5\/16\/2012<\/td>\nClinical Trials: Budgeting and Billing<\/strong>
\nEllen Jamieson, MS, MBA and Alex Hui, BA<\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
4\/18\/2012<\/td>\nUnderstanding and Complying with NIH Public Access Policy
\n<\/strong>Young-Joo Lee, MIS<\/td>\n		Slides<\/a>
\nVideo<\/a><\/td>\n<\/tr>\n
3\/21\/2012<\/td>\n Responsible Conduct of Research (RCR) Instruction on Authorship: What, Why, How
\n<\/strong> Susan Frey, MAT, JD<\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
2\/15\/2012<\/td>\n The Certificate of Confidentiality: One Research Team’s Experience
\n<\/strong> Christine Baugh, BA<\/td>\n		No Slides
\nVideo<\/a><\/td>\n<\/tr>\n
1\/18\/2012<\/td>\nResponsible Conduct of Research (RCR): What all Researchers Need to Know
\n<\/strong> Susan Frey, MAT, JD<\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
12\/21\/2011<\/td>\nAddressing Intimate Partner Violence in the Health Care Setting: Implications for Research
\n<\/strong> Joanne Timmons, MPH<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
11\/16\/2011<\/td>\nUnique Challenges in Obtaining Valid Samples in Internet Research
\n<\/strong> Wendy Coster, PhD, OTR\/L, FAOTA and Amy Rubin, PhD<\/strong><\/td>\n		No Slides<\/td>\n<\/tr>\n
10\/19\/2011<\/td>\nThe Grant Creation Process: 10 Easy Steps to Coordinating and Completing a Federal Grant for your PI\u00a0\u00a0<\/strong>Maura Harrington, MIIM<\/strong><\/td>\nSlides<\/a><\/td>\n<\/tr>\n
9\/21\/2011<\/td>\nCan Migration Studies Help us Understand Asthma in Children
\n<\/strong>Doug Brugge, JD<\/strong><\/td>\n		No Slides<\/td>\n<\/tr>\n
6\/15\/2011<\/td>\nMinimizing Variability in Trials that Use Clinician Assessed Endpoints
\n<\/strong> Harry Barnett, JD<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
5\/18\/2011<\/td>\nHelp your Subjects Understand your Study
\n<\/strong> Michael Paasche-Orlow, MD, MA, MPH<\/strong><\/td>\n		No Slides
\n <\/a><\/td>\n<\/tr>\n
4\/20\/2011<\/td>\nCommunity Engagement in Research
\n<\/strong> Ester Shapiro, JD<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
3\/16\/2011<\/td>\nBU\/BMC Recruitment Basics
\n<\/strong> Kimberly Russell-Lucas, MPH, CCRP<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
2\/16\/2011<\/td>\nWriting Grants: Human Subjects Protection and DSMPs
\n<\/strong> Maura Harrington, MIIM<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
1\/19\/2011<\/td>\nPreparation for an FDA Inspection: Clinical Research Sites
\n<\/strong>Michelle Noe, MBA, RD<\/td>\n		Slides upon request<\/td>\n<\/tr>\n
12\/15\/2010<\/td>\nRules of Engagement: Collaborating with Non BU\/BMC Investigators<\/strong>
\nMary Banks, RN, BSN<\/strong><\/td>\n		Slides<\/a>
\n <\/a><\/td>\n<\/tr>\n
11\/17\/2010<\/td>\nInformed Consent in Clinical Research: Fantasy, Illusion or Reality?
\n<\/strong> James Hyde<\/strong><\/td>\n		Slides<\/a>
\n <\/a><\/td>\n<\/tr>\n
10\/20\/2010<\/td>\nRecruitment, Retention and Reporting Issues in an International Longitudinal Study
\n<\/strong> James Burns, ScD<\/strong><\/td>\n		No Slides<\/td>\n<\/tr>\n
9\/15\/2010<\/td>\nCollecting Genes and Informed Consent: Lessons from the Havasupai, Berkeley, 23&Me, and the Minnesota State Fair
\n<\/strong> George J. Annas, JD, MPH<\/strong><\/td>\n		No Slides<\/td>\n<\/tr>\n
6\/16\/2010<\/td>\nDSMBs and Research Study Stopping Rules
\n<\/strong> Theodore Colton, ScD<\/strong><\/td>\n		Slides<\/a>
\n <\/a><\/td>\n<\/tr>\n
5\/19\/2010<\/td>\nRecruitment and the CRRO Registry
\n<\/strong> Kimberly Russell, MPH, CCRP<\/strong><\/td>\n		No Slides<\/td>\n<\/tr>\n
4\/21\/2010<\/td>\nApproaches to Qualitative Research
\n<\/strong> Sharlene Hesse-Bieber, PhD<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
3\/17\/2010<\/td>\nFocusing on Focus Groups
\n<\/strong> Lee Strunin, PhD<\/strong><\/td>\n		No Slides<\/td>\n<\/tr>\n
2\/17\/2010<\/td>\nSuccessful Recruitment of Older Research Participants: Lessons from the Harvard Cooperative Program on Aging
\n<\/strong> Marcie Becker Freeman, MEd<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
1\/20\/2010<\/td>\nResearch with Immigrant Populations
\n<\/strong> Alex Pirie, BA<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
12\/16\/2009<\/td>\nLiability and Compensation Issues in Research
\n<\/strong> Wendy Mariner, JD, MPH<\/strong><\/td>\n		<\/td>\n<\/tr>\n
11\/18\/2009<\/td>\nA Town Hall Meeting with IDS
\n<\/strong> HyeSeon Hong, PharmD<\/strong><\/td>\n		Slides<\/a>
\n <\/a><\/td>\n<\/tr>\n
10\/21\/2009<\/td>\nIs it Ethical to Conduct Research on Subjects who Cannot Consent? The Conundrum of Research with Children and Incompetent Individuals
\n<\/strong> Leonard Glantz, JD<\/strong><\/td>\n		<\/td>\n<\/tr>\n
9\/16\/2009<\/td>\nFDA Regulation: Don’t Drown in the Regulatory Sea?
\n<\/strong> Patricia Bass, JD, MPH<\/strong><\/td>\n		Slides<\/a>
\n Video<\/a><\/td>\n<\/tr>\n
6\/17\/2009<\/td>\nDeveloping Budgets for Research Projects with a Focus on Phase 3 Clinical Trials
\n<\/strong> Olivera Vragovic, MBA<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
5\/20\/2009<\/td>\nJust Because You Can’t Count It Doesn’t Mean it Doesn’t Count: Good Research with Qualitative Data
\n<\/strong> Don Allensworth-Davies, MSc and Jenniffer Leyson, MA<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
4\/15\/2009<\/td>\nInvestigator Responsibilities and First-time INDs: Two Accounts of the Process
\n<\/strong> Lori Gilmartin, RN, BSN; Hatice Hasturk, DDS, PhD; Carine Lenders, MD<\/strong><\/td>\n		Slides 1<\/a>
\n Slides 2<\/a>
\nSlides 3<\/a><\/td>\n<\/tr>\n
3\/18\/2009<\/td>\nPitfalls in Survey Research
\n<\/strong> Thomas W. Mangione, PhD<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n
2\/18\/2009<\/td>\nThe Polio Crusade: A Video Documentary on the Polio Vaccine and
\nDiscussion of the Ethics of the Largest Public Health Experiment in American History
\n<\/strong> Moderators: Mary-Tara Roth, RN, MSN, MPH and Mary Banks, RN, BSN<\/strong><\/td>\n		N\/A<\/td>\n<\/tr>\n
1\/21\/2009<\/td>\nObedience to Authority: The Milgram Experiment and Its Contemporary Replication –
\nWas it Ethical Then? Is it Ethical Now?\u00a0\u00a0<\/strong>Susan S. Fish, PharmD, MPH<\/strong><\/td>\n		Slides<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

        Date Title and Presenter Materials 4\/22\/2026 Informed Consent Form Readability as Ethical Practice Stephanie Warth – Human Subjects Research Education Manager, CRRO Video Slides 3\/25\/2026 The Importance of Protocol Adherence: Why it Sometimes Doesn’t Happen and How to Ensure it Does! Mary-Tara Roth, RN, MSN, MPH – Director, Clinical Research Resources […]<\/p>\n","protected":false},"author":1250,"featured_media":0,"parent":2445,"menu_order":14,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"_links":{"self":[{"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/pages\/232"}],"collection":[{"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/users\/1250"}],"replies":[{"embeddable":true,"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/comments?post=232"}],"version-history":[{"count":57,"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/pages\/232\/revisions"}],"predecessor-version":[{"id":7113,"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/pages\/232\/revisions\/7113"}],"up":[{"embeddable":true,"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/pages\/2445"}],"wp:attachment":[{"href":"https:\/\/www.bumc.bu.edu\/crro\/wp-json\/wp\/v2\/media?parent=232"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}