- University of Rochester (Rochester, NY)
- …which may include multiple site human subject studies. May provide training on federal, state, sponsor and/or institutional regulations, policies and practices ... forms (CRFs) and study-specific procedure manuals and documents. Clinical trials coordinator II for the University of Rochester Translational Pain Research Program.… more
- University of Rochester (Rochester, NY)
- …and/or other interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board (IRB), Sponsor, and/or any other ... such as study drugs and devices. + Ensures additional training is provided to ensure changes to protocol and...completion of 6 months in the Human Subject Research Coordinator Trainee program required + Or equivalent combination of… more