Assists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within department
Job Summary
Assists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within department.
Maintains protocol amendments, deviations, and informed consent changes regarding oncology research studies, assures all documentation is managed compliantly and maintained in an audit-ready manner.
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Matching Summary
Assists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within department.