The University of Mississippi Medical Center requires all individuals directly involved in the conduct of human subjects research to complete human subjects protection training before study involvement may begin. Institutional Review Board (IRB) approval will be withheld until the training requirement has been met by the Principal Investigator.
This requirement applies to all persons who have a significant role in the research. All of these individuals should be listed as study personnel in the IRB application.Examples include:
The CITI initial Human Subjects Research course (either biomedical or social-behavioral)