DescriptionThe Department of OBGYN is seeking to hire a full time Clinical Research Coordinator to be responsible for regulatory coordination of complex clinical research studies. In this role you will perform detailed reviews of clinical research protocols and utilizes that information to prepare, manage and submit all required study/regulatory documents and all required applications and forms related to internal UCLA requirements, FDA requirements, sponsor requirements, etc. Works with study monitors to process, review and collect the appropriate regulatory documents in a timely manner and in compliance with federal, state, and university mandated laws, regulations and policies.