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Principal Clinical Data Manager
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- Serve as lead CDM on assigned clinical trials by attending internal and external clinical trial project team meetings.
- Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer documents including import/export agreements and data specifications.
- Provide ad-hoc report development, and support database lock and archiving activities.
- Ensure that medical coding is completed in a timely fashion, completed for all data cuts, and reviewed and approved by medical monitors.
- Ensure project documentation is being archived in a timely manner into the Trial Master File.
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