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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 quality assurance auditors. My primary focus is to ensure clinical trial sponsors provide quality systems in managing clinical trials that protects the safety of subjects/patients and that the data colleted is of the highest integrity.
Clinical Research
About Me
Industry: |
Science & Biotech |
|---|---|
Occupation: |
Clinical Research |
Education level: |
Certification |
Will Relocate: |
Yes |
