Past seminars
| Seminar date | Seminar title and Speaker(s) | Slide PDFs and Videos
(as available) |
| 3/20/2013 | Tissue and Data Repositories, Part 2: Banks on Banks Data and Tissue Repositories, Part 2Data and Tissue Repositories, Part 2 Mary Banks, RN, BSN |
Slides |
| 2/20/2013 | Data and Tissue Repositories, Part 1 Data and Tissue Repositories, Part 1
Patricia Bass, JD, MPH |
Slides |
| 1/16/2013 | Community Based Participatory Research: Training Community Workers to Engage in Research
Brenda Heaton, PhD, MPH |
Slides |
| 12/19/2012 | Child Abuse Reporting Requirements in the Research Context
Robert Sege, MD, PhD |
Slides |
| 11/14/2012 | Recruiting Subjects: How the ReSPECT Registry and Study Finder can Help
Farrah Belizaire, BS; R. Joshua Reynolds, BS; Mary-Tara Roth, RN, MSN, MPH |
Slides |
| 10/17/2012 | The BMC Clinical Data Warehouse Clinical Data Warehouse: An Overview of the Possibilities for Research using the Clinical Data Warehouse
Linda Rosen, MSEE |
Slides |
| 9/19/2012 | An Overview of the Changes in Conflict of Interest Regulation and How It Affects Your Research Getting Conflicts: An Overview of the Changes in Conflict of Interest Regulation and How it Affects Your Research
Jodi R. Edelstein, JD |
Slides |
| 6/20/2012 | The BUMC Research Occupational Health Program The Research Occupational Health Program at BU/BMC
Thomas Winters, MD, FACOEM and Sandra Reno, RN |
Watch Video |
| 5/16/2012 | Grants Update Clinical Trials – Budgeting and Billing
Ellen Jamieson, MS, MBA and Alex Hui, BA |
Slides Watch Video |
| 4/18/2012 | Understanding and Complying with NIH Public Access Policy
Young-Joo Lee, MIS |
Slides |
| 3/21/2012 | Responsible Conduct of Research Instruction on Authorship: What, Why How
Susan Frey, MAT, JD |
Slides |
| 2/15/2012 | The Certificate of Confidentiality: One Research Team’s Experience
Christine Baugh, BA |
No Slides |
| 1/18/2012 | Responsible Conduct of Research: What all Researchers Need to Know
Susan Frey, MAT, JD |
Slides |
| 12/21/2011 | Addressing Intimate Partner Violence in the Health Care Setting: Implications for Research
Joanne Timmons, MPH |
Slides |
| 11/16/2011 | Unique Challenges is Obtaining Valid Samples in Internet Research
Wendy Coster, PhD, OTR/L, FAOTA and Amy Rubin, PhD |
No Slides |
| 10/19/2011 | The Grant Creation Process: 10 Easy Steps to Coordinating and Completing a Federal Grant for your PI
Maura Harrington, MIIM |
Slides |
| 9/21/2011 | Can Migration Studies Help us Understand Asthma in Children?
Doug Brugge, PhD |
No Slides |
| 6/15/2011 | Minimizing Variability in Trials that Use Clinician Assessed Endpoints
Harry Barnett, JD |
Slides |
| 5/18/2011 | Help your Subjects Understand your Study
Michael Paasche-Orlow, MD, MA, MPH |
No Slides |
| 4/20/2011 | Community Engagement in Research
Ester Shapiro, PhD |
Slides |
| 3/16/2011 | BU/BMC Recruitment Basics
Kimberly Russell-Lucas, MPH, CCRP |
Slides |
| 2/16/2011 | Writing Grants: Human Subjects Protection and DSMPs
Maura Harrington, MIIM |
Slides |
| 1/19/2011 | Preparation for an FDA Inspection: Clinical Research Sites
Michelle Noe, MBA, RD |
Slides upon request |
| 12/15/2010 | Rules of Engagement : Collaborating with Non BU/BMC Investigators
Mary Banks, RN, BSN |
Slides |
| 11/17/2010 | Informed Consent in Clinical Research: Fantasy, Illusion, or Reality?
James Hyde |
Slides |
| 10/20/2010 | Recruitment, Retention, and Reporting Issues in an International Longitudinal Study
Jane Burns, ScD |
NA |
| 9/15/2010 | Collecting Genes and Informed Consent: Lessons from the Havasupai, Berkeley, 23&Me, and the Minnesota State Fair
George J. Annas, JD, MPH |
Watch Video |
| 6/16/2010 | DSMBs and Research Study Stopping Rules
Theodore Colton, ScD |
Slides |
| 5/19/2010 | Recruitment and the CRRO Registry
Kimberly Russell-Lucas, MPH, CCRP |
No Slides |
| 4/21/2010 | Approaches to Qualitative Research
Sharlene Hesse-Bieber, PhD |
Slides |
| 3/17/2010 | Focusing on Focus Groups
Lee Strunin, PhD |
NA |
| 2/17/2010 | Successful Recruitment of Older Research Participants: Lessons from the Harvard Cooperative Program on Aging
Marcie Becker Freeman, Med |
Slides |
| 1/20/2010 | Research with Immigrant Populations
Alex Pirie, BA |
Slides |
| 12/16/2009 | Liability and Compensation Issues in Research
Wendy Mariner, JD, MPH |
Watch Video |
| 11/18/2009 | A Town Hall Meeting with IDS
HyeSeon Hong PharmD |
Slides |
| 10/21/2009 | Is it Ethical to Conduct Research on Subjects who Cannot Consent? The Conundrum of Research with Children and Incompetent Individuals
Leonard Glantz, JD |
Watch Video |
| 9/16/09 | FDA Regulation: Don’t Drown in the Regulatory Sea? Patricia Bass, JD, MPH |
Slides |
| 6/17/2009 | Developing Budgets for Research Projects with a Focus on Phase 3 Clinical Trials Olivera Vragovic, MBA | Slides |
| 5/20/2009 | Just Because You Can’t Count It Doesn’t Mean It Doesn’t Count: Doing Good Research with Qualitative Data
Don Allensworth-Davies, MSc and Jenniffer Leyson, MA |
Slides |
| 4/15/2009 | Investigator Responsibilities and First-time INDs: Two Accounts of the Process
Lori Gilmartin, RN, BSN; Hatice Hasturk, DDS, PhD; Carine Lenders, MD |
Slides 1 |
| 3/18/2009 | Pitfalls in Survey Research
Thomas W. Mangione, PhD |
Slides |
| 2/18/2009 | The Polio Crusade: A Video Documentary on the Polio Vaccine and Discussion of the Ethics of the Largest Public Health Experiment in American History
Moderators: Mary-Tara Roth, RN, MSN, MPH and Mary Banks, RN, BSN |
|
| 1/21/2009 | Obedience to Authority: The Milgram Experiment and Its Contemporary Replication – Was it Ethical Then? Is it Ethical Now?
Susan S. Fish, PharmD, MPH |
Slides |
| 12/17/2008 | Financial Conflicts of Interest in Clinical Research
Susan H. Frey, JD |
|
| 11/19/08 | Industry-Sponsored Clinical Research at BUMC: An Introduction
Jane Kinsel, PhD |
Slides |
| 10/15/2008 | Tissue and Data Banking: An Essential Ingredient for Genetic Research
P. Pearl O’Rourke, MD |
Slides |
| 9/17/08 | The Language of Consent: Using the Short Form in Consenting Non-English Speakers in Clinical Research
Mary Banks, RN, BSN |
Slides |
| 6/18/2008 | Using the Internet to Conduct Research and Recruit Subjects
Christine Chaisson, MPH and Don Allensworth-Davies, MSc |
Slides |
| 5/21/2008 | Minding the p-values and Quartiles: Study Design, Data Analysis, and the IRB
Don Allensworth-Davies, MSc |
Slides |
| 4/30/2008 | Focus Group Interviewing in Research
Lee Strunin, PhD |
Slides |
| 4/16/2008 | Informed Consent: Moving from Readability to Comprehension
Michael Paasche-Orlow, MD, MA, MPH |
Slides |
| 3/19/2008 | BMC Research Pharmacy Update
HeySeon Hong, PharmD |
Slides |
| 2/27/2008 | BMC Clinical Research Policy and Procedures: Billing Ancillary Hospital Services
Ellen N. Jamieson, MS, MBA and Alexandria Hui |
Slides 1 |
| 2/20/2008 | Confidentiality/Non-Disclosure Agreements with Industrial Research Sponsors
Karen A. Mullin, JD, LLM |
|
| 1/16/2008 | Entrusted: The 60-year Dialogue of Informed Consent at the Framingham Heart Study
Greta Lee Splansky, MS; Sue Blease, BDS, MPH; Margaret Kelly-Hayes, EdD, RN, FAAN |
Slides |
| 12/19/2007 | Accessing and Scheduling Radiology Research at BUMC
Jorge A. Soto, MD and Kirise Kramer, BA |
|
| 11/14/2007 | Reporting Unanticipated Problems and Adverse Events: A Change in Policy
Mary Banks, RN, BSN |
Slides |
| 10/17/2007 | Case Report Forms: A Critical Link to the Success of Your Research Study
Alice B. Bisbee, MPH |
Slides |
| 9/19/2007 | An Interactive Approach to Good Clinical Practice (GCPs)
Brandi N. Ring, MA |
Slides |
| 6/18/2007 | Dispelling Common Myths about the BUMC IRB
Mary Banks, BS, RN, BSN |
Slides |
| 5/21/2007 | Investigator Initiated Studies: Risks, Benefits, and Rewards
Lori Gilmartin, RN, BS |
Slides |
| 4/11/2007 | Accessing Data for Clinical Research: The Boston Medical Center Clinical Data Warehouse
Linda Rosen, MSEE and Richard Saitz, MD, MPH |
Slides |
| 3/21/2007 | The Right Prescription for Working with Investigational Drug Service at BMC
HyeSeon Hong, PharmD |
Slides |
| 2/21/2007 | Fraud in Medical Research: Data Falsification and Data Fabrication in Clinical Trials
Theodore Colton, ScD |
Slides |
| 1/17/2007 | When the Subject Can’t Consent
Mary Banks, RN, BS |
Slides |
| 11/15/2006 | Planning for Data and Safety Monitoring: Developing Your Study-specific DSMP
Mary-Tara Roth, RN, MSN, MPH |
Slides |
| 10/18/2006 | Enrolling Non-English Speakers into Research Studies
Judith Bernstein, RN, PhD and Edward Bernstein, MD |
Slides |
| 9/20/2006 | Preparing for an FDA Audit
Carol Gloff, PhD |
Slides |
| 6/21/2006 | Making Sense of the Ethics of Research that Involves Persons who Cannot Give Informed Consent
Jason Karlawish, MD |
|
| 5/17/2006 | Moving from Readability to Comprehension
Michael Paasche-Orlow, MD, MA, MPH |
Slides |
| 4/19/2006 | FDA Quick Guide: What Every Investigator Should Know about Drug and Medical Device Research
Patricia Bass, JD, MPH |
Slides |
| 2/15/2006 | Got Data? Tips for Researchers on Completing the Data Analysis Section of the IRB Application
Don Allensworth-Davies, MSc. |
|
| 1/18/2006 | IRB Update 2006!
Mary Banks, RN, BSN |
|
| 12/2005 | Research Subject Retention: Strategies for Success | |
| 10/19/2005 | Successful Subject Recruitment Strategies
Richard Saitz, MD, MPH; Joyce Goggins, MPH; Mary-Tara Roth, RN, MSN, MPH; Edward Bernstein, MD |
Slides 1 |
| 9/05 | Responsible Conduct of Research: An Overview
Susan S. Fish, PharmD, MPH |
