This course is part of the ITHS Competency-Based All-Level Training (COBALT) Curriculum for Research Coordinators. It aligns with Domain 2 of the JTF Competency Framework.
This course provides an overview of the PI's responsibilities for managing adverse events in a clinical trial. Dr. Paul Martin reviews key definitions, distinguishes between the terms "severe" and "serious," and examines how adverse events should be assessed and documented.
Author: Fred Hutch Clinical Research Support (CRS) with Paul Martin, MD
Duration: Approximately 25 minutes
RC LEVEL 1, 2, 3
This opportunity is open to all eligible persons regardless of race, sex or other identity.
- Instructor: ITHS Education Team