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Regulatory Specialist- CRI
Your Job: Under the direct supervision of the Clinical Research Institute (CRI) Director the Regulatory Specialist will perform expertise in the regulatory component of all clinical research trials to include, but not limited to; Phase II and IV clinical, investigator initiated trials (IITs), and retrospective analysis of clinical data.Your Job Requirements: Bachelor's degree required, Master's degree preferred CCRC or CCRP (preferred)GCP certification (preferred) Firm knowledge of computer skills One year of experience in a medical or clinical setting (required) One year of experience in clinical research and experience in research regulatory affairs (required)

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