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Clinical Trial ManagerCleveland, OH- Anticipate and resolve project needs - Ensure case report forms meet project?s needs - Assist in protocol development - Coordinate investigator meeting - Prepare project timelines - Locate appropriate investigators and negotiate budgets/clinical study agreements - Prepare appropriate documents for the IRB and the FDA - Ensure completion of all final and interim reports required by the sponsor - Serve as primary contact with sponsor - Oversee study budget - Develop and maintain Study Master File - Perform other duties as assigned by management Job Requirements: - Bachelor in Life Sciences or a related field - Minimum 7 and 3 years? clinical trial and monitoring experience respectively - Minimum 2 years' project management experience - Working knowledge of contract - Proven...originally from The Job Spider - More Tools...
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