Study Coordinator
McKesson(1 month ago)
About this role
The Study Coordinator at Sarah Cannon Research Institute supports the execution and monitoring of Phase I–IV clinical research protocols within a community-based oncology research network. The role works with investigators, sponsors, and clinical teams to maintain data integrity, regulatory compliance, and participant safety. It advances clinical trial operations that contribute to developing new cancer therapies.
Required Skills
- Clinical Trials
- Patient Eligibility
- Protocol Compliance
- Adverse Events
- Data Entry
- EDC Systems
- FDA Guidelines
- GCP
- Source Documentation
- Monitoring Visits
+2 more
Qualifications
- Bachelor's Degree (Preferred)
About McKesson
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