Institutional Review Board
Past Presentations

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ViewThe Pre-review Process and SMOG: An OverviewLaura Renner, External Consultant04/28/2008
ViewThe Vanderbilt Research Advocacy ProgramJan Zolkower, BS, CIP, CCRP - Research Advocacy Officer02/25/2008
View,View,View,ViewNews You Can Use: Mobile Devices and Data Security (Part 1)Salvador Ortega (Network Security); Gaye Smith (Privacy Officer); and Gene Gallagher (IRB)01/31/2008
ViewQuestionnaire DesignTheresa A. Scott, M.S. - Department of Biostatistics01/28/2008
ViewClinical Research Staff Council meeting: Cochair elections, StarBRITE: What is it and how can it help me?Tara Holmes, and Gail Mayo, Research Support Services01/18/2008
ViewClinical Research Staff Council Meeting: What the research team needs to know about HIPAA and the privacy policyGaye Smith, MBA, Privacy Officier10/19/2007
ViewIRB Essentials: Humanitarian Use Device IssuesBecca DuBose, BS, CCRP, CIP07/30/2007
ViewNews You Can Use: What's in your freezer: Do you know everything you need to know about specimen/data repositories?M. Kay Washington, M.D., Ph.D., Director of Surgical Pathology06/07/2007
ViewStandard Operating Procedures in Clinical ResearchKaren Majchrzak02/22/2007
ViewClinical Research Staff Council Meeting: Navigating through the contracts processLibby Salberg, JD, Associate Director, GCM02/15/2007
ViewChanges, Changes, and More Changes: Learn about new standard operating procedures for the clinical labScott Ratchford01/24/2007
ViewResearch Support Services Presents: Statistics for DummiesRachel Enriquez, RN, PhD01/12/2007
ViewNote: This session is now full and registration has been closed.
News You Can Use: VU Research Conducted at the VA: What VU Researchers Need to Know
Dr. Gordon Bernard, MD12/07/2006
ViewResearch Support Services Presents: Statistics for DummiesRachel Enriquez, RN, PhD10/26/2006
ViewAfternoon Delight Series: Project IMPACTT Supporting Research Excellence A research team's perspectiveTerri Edwards, RN,
Kurt Spindler, MD
Tara Holmes, PA-C, MPH
Laura Huston, MS
10/20/2006
ViewNews You Can Use: Writing an Informed Consent DocumentTodd Rice, MD, MSc07/10/2006
ViewClinical Research Staff Council Meeting: Medications and the Clinical TrialGeri Foster, DPh, Investigational Drug Pharmacy06/15/2006
ViewIRB Essentials: What You Need to Know When a Participant Becomes Incarcerated or When Enrolling a Prisoner PopulationJan Zolkower, BS, CTR, CIP05/22/2006
ViewClinical Research Staff Council Meeting: Can Type 2 Diabetes really be a Surgical Problem? Erik Hansen, MD, MPH
Fellow in Surgical Research
 
05/18/2006
ViewThe Redesign of Billing Compliance: Learn about the new patient tracking system and new research billing requirementsKelly Willenberg, RN, MBA04/27/2006
ViewNYCU - When a Student Becomes the ResearcherDavid G. Schlundt, Ph.D.03/31/2006
ViewIRB Essentials: Let's Write an IRB ProtocolNila Sathe, MA, MLIS and Jan Zolkower, BS, CTR, CIP02/27/2006
ViewWhen Participants or Others Have Research Related Complaints: The Next StepDenise Roe, BA, CCRP, CIP and Jan Zolkower, CTR, CIP12/09/2005
ViewIRB Essentials: The Consent Process: It Keeps Going and Going...Wendy Lloyd, LPN, CCRP11/28/2005
ViewHIPAA and the New Covered EntityGaye Smith
VUMC Privacy Official
11/03/2005
ViewClinical Research Staff Council Meeting: Hot Topics in in Clinical Research in Billing and Compliance Kelly Willenberg, RN, MBA10/20/2005
ViewNeed Research Volunteers? Learn about new initiatives that can help you identify and recruit research participants. Paul Harris, PhD09/21/2005
ViewClinical Research Staff Council Meeting: Experience with the RSV Allergy Study and Recruitment and Retention of Spanish Speaking Families Rachel Enriquez, RN, PhD09/15/2005
ViewIRB Essentials: Writing an IRB ProtocolJan Zolkower, CTR, CIP and Nila Sathe, MA, MLIS08/29/2005
ViewWriting an Informed Consent DocumentTodd Rice, MD, MSc08/11/2005
ViewIRB Essentials: A Little Exposure - the HSRC and the RDRCDena Johnson, BA, CIP and David Hiller, EMT, RN06/27/2005
ViewClinical Research Staff Council Meeting: Sham Surgery and Placebo Control TrialsThomas Talbot, MD, Assistant Professor of Medicine & Preventive Medicine06/16/2005
ViewWho's The Boss?: The Role of The Study CoordinatorJulie McFarlane, RN, BSN, Tonya Yarbrough, RN, and Jill Janssen, RN, BSN06/03/2005
ViewIRB News You Can Use: Outside Safety Reports, When Will They End?Denise Roe, BA, LPN, CIP and Julie Ozier, CCRC, CIP05/26/2005
ViewIRB Essentials: Preparing for an IRB AuditByron Kaelin, RN, CIP05/23/2005
ViewClinical Research Staff Council Meeting: IATA Regulations: Are you compliant when shipping samples?
LouAnn Burnett, Biological Safety Officer05/19/2005
ViewBy George! I Think We've Got It: An Introduction to Tech Transfer and Conflicts of InterestBrian Laden, Tom Noland, Tom Hazinski, and moderated by Gordon Bernard05/12/2005
ViewOh Behave! : Introduction to the Responsible Conduct of ResearchElizabeth Heitman, Ph.D., Associate Professor of Medical Ethics, Center of Clinical and Research Ethics04/28/2005
ViewClinical Research Staff Council Meeting: Vanderbilt Nursing - Our Magnet JourneySabrina Downs, RN, Magnet Recognition04/21/2005
ViewI'm Just A Bill: Preparing For a Clinical Trial Billing AuditKelly Willenberg, BSN, MBA, Manager, Clinical Research Financial Compliance 04/19/2005
ViewDevice Advice: Understanding the Institutional Requirements of Using Medical DevicesStephanie Randa and Kelly Willenberg03/31/2005
ViewHow Much Is This Going to Cost Me?: Building a Clinical Trial BudgetKelly Willenberg, BSN, MBA, Manager, Clinical Research Financial Compliance03/15/2005
ViewDreams Can Come True: Introducing the Clinical Research Staff CouncilGordon Bernard, MD, Assistant Vice Chancellor02/17/2005
ViewSign on the Dotted Line: The Fundamentals of Clinical Trial Contracts and Related Agreements Libby Salberg, J.D., Office of Grants and Contracts Management , Associate Director02/16/2005
ViewOffice of Research Town Hall Meeting: Conducting Clinical Research at VanderbiltGordon Bernard, M.D. Assistant Vice Chancellor01/25/2005
ViewDon't Be Afraid of the Big Bad Wolf: Preparing for an FDA AuditAlice Owens-Gatlin, J.D., C.C.R.P.12/08/2004
ViewOops...Did I Do That: An Overview of FDA/OHRP determination lettersQuincy J. Byrdsong11/08/2004
ViewNews You Can Use - You Think YOU Got Problems: Revised Reporting for Adverse EventsDenise Roe - IRB Associate Director09/24/2004
ViewNews You Can Use - You Think YOU Got Problems: Revised Reporting for Adverse EventsDenise Roe - IRB Associate Director09/24/2004
ViewIRB Brown Bag: IMPACTT Your Research, IRB Measured Performance and Collaborative Training: Terri Hagan09/15/2004