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Regional Clinical Monitoring, Kansas City, MO

To monitor clinical trials of all phases using extensive knowledge of drug development and regulatory processes. Experience: - study site selection and set up – preparation of pre-study regulatory documentation - preparation of site monitoring reports in accordance with specific timelines - follow-up and resolution of sites issues - identifies and assists sites with DCF resolution - maintains regular contact with ...

Tags for this Online Resume: Clinical Trial Manger, Clinical Research Associate (CRA), Medical Writer (MW), Project Manager, Clinical Research Scientist, Clinical Operation