Who is considered key study personnel (KSP) according to UTHSC?
For the purpose of completing section 3.0 of the IRB electronic application, the designation “key study personnel” includes all persons who will have a significant role in the design or conduct of the research, and includes at a minimum all principal investigators and co-investigators, any individuals who are individually named on a grant or contract application, persons who are listed on an FDA form 1572, research coordinators, persons who supervise those who obtain informed consent, individuals who obtain informed consent, and those who are named as contact persons in the informed consent documents or recruitment materials for research.
