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Online Resumes with "ICH GCP compliance"
Clinical Research Professional- 20 years experience- Memphis
Clinical research professional with over 20 years of experience in both industry and academia. Responsible for all audit activities for multiple phase 1-3 clinical trials. Responsibilities include but are not limited to ICH/GCP compliance. Reviews key study documents such as protocols, informed consents, CRFs, monitor reports, and CSR. Presents protocol and GCP training at Investigator meetings. Mentors and trains junior qu...
Tags for this Online Resume: GCP, FDA submission documents, Drug safety, GLP, NDA, Auditor
