Grand Rounds: Investigator Responsibilities in Clinical Trials

Marie Rape, RN, BSN, CCRC

Associate Director, Regulatory Service
NC TraCS Institute

Objectives:

1. Understand the role & responsibility of the PI in Good Clinical Practice
2. Recognize FDA’s requirements and expectations for PI oversight, PI responsibilities
3. Create process to document PI oversight and supervision of research

321 MacNider Hall
Thursday, March 15, 2018, 8:00 AM

Sponsored by the School of Medicine of The University of North Carolina at Chapel Hill.