NextGen Clinical Trial Investigator Training - Session 5, September 1
The NextGen Clinical Trial Investigator Training is a five-session educational program designed for faculty who are either involved in clinical trials or who would like to become involved. The series includes lectures and panel discussions from leaders across the University of Missouri System, as well as Washington University in St. Louis, to define the regulatory, operational and ethical components of clinical trials, with the goal of developing a skilled workforce that provides the highest level of patient safety, teamwork and data quality. The program also covers institution-specific resources for investigators.
Timeframe: Five weeks, starting Aug. 4 through Sept. 1, 4:30 to 7:30 p.m.
August 4 - Session 1: Good Clinical Practice & Team Science
August 11 - Session 2: What is a Clinical Trial?
August 18 - Session 3: Patient & Community Engagement & Responsible Conduct of Research
August 25 - Session 4: Research Funding & Team Management
September 1 - Session 5: Institutional Resources
Session 5: Institutional Resources
|Office of Research & Economic Development (ORED) – Susan Renoe, PhD, Assistant Vice Chancellor for Research, Extension & Engagement, Office of Research and Economic Development and the Office of Extension & Engagement, University of Missouri-Columbia|
|Office of Rural Health – Kathleen Quinn, PhD, Associate Dean for Rural Health and Director of the Rural Scholars Program, University of Missouri – Columbia School of Medicine|
|IRB Review & Oversight – Lori Wilcox, EdD, Director of Human Subjects Research Protections Program, University of Missouri – Columbia Institutional Review Board in the Office of Research and Economic Development|
|Common Mistakes Made in Clinical Trials (Institution Trends) – Hope Gole, PhD, Associate Director of Research Activities, University of Missouri-Columbia School of Medicine MU, and Dyann Helming, MSN, APRN, Clinical Nurse Specialist, Adult Health, and Director of Research Operations & Planning, University of Missouri Clinical Research Center|
|Grant Writing Support – Martha Brendel, Grant Writer Lead, Medical Research Office, University of Missouri-Columbia School of Medicine|
|Library Resources for the Research Cycle – Rachel Alexander, Research Support Librarian, J. Otto Lottes Health Science Library, University of Missouri-Columbia|
|OSPA & Regulatory Guidelines – Brenda Leuenberger, Associate Director, Pre-Award, Office of Sponsored Programs Administration, University of Missouri – Columbia Institutional Review Board in the Office of Research and Economic Development|