Onsite Clinical Research Regulatory Coordinator I

A major research university in Florida is seeking a Clinical Research Regulatory Coordinator I to support its Clinical Research Support Enterprise. This role involves maintaining regulatory documentation, preparing IRB submissions, and assisting with informed consent documents. Candidates must have a High School diploma or GED. This position requires on-site work days and does not offer remote options. It's an opportunity to contribute to significant clinical research initiatives within a prominent institution. #J-18808-Ljbffr