The Protocol/Operations Coordinator is responsible for preparing documentation for industry sponsored, investigator initiated, and national cooperative group clinical trials. The position will prepare IRB documents and other study-related tools for the start-up and management of clinical trials including the IRB application, consent form, study synopsis, annual renewals, modifications, eligibility checklists, and study management tools. The incumbent will report to the CRS Regulatory Operations Manager.
Experience and Abilities
Knowledge and Skills