Regulatory assistant - ccc clinical trials office
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- Assists with regulatory functions in support of clinical research activity.
- Assists in preparation of protocol submissions to Institutional Review Boards (IRBs) and provides updates on submission status
- Assists in preparation of other required regulatory documents
- Distributes approved documents
- Relays information to clinical research staff
- Assists with data entry including collecting, entering and maintaining data and documents in the OnCore electronic database
- Assists with monitoring visits
- Assists with regulatory issues
- Creates and maintains regulatory files
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