Clinical Research and Human Protection Training
This PowerPoint is designed as a template for investigators to provide standardized training for participating clinicians and clinical research assistants on the: 1- clinical trial objectives and design, 2- protocols to follow during the clinical trial, and 3- and also to provide basic consent and human protection (IRB) training for participating clinical staff. This training PowerPoint can be used during training of the clinicians and clinical research assistants, and it can also be used over the course of the clinical trial to maintain adherence to the clinical trial protocol. The IRB training materials can be used to train participating clinicians and clinical research staff that will be working directly with the patients enrolled in the study.
Visit the Office of Research and Innovation for more information.