Study Coordinator
McKesson(1 month ago)
About this role
The Study Coordinator at Sarah Cannon Research Institute supports oncology clinical research within a community-based network, contributing to the execution and integrity of Phase I–IV trials. This role interfaces with investigators, sponsors, and internal teams to support the institute’s mission of advancing cancer therapies. It is positioned within the research organization and focuses on enabling high-quality clinical investigations.
Required Skills
- Clinical Trials
- Patient Eligibility
- Data Entry
- Safety Reporting
- Protocol Compliance
- EDC
- Regulatory Compliance
- Monitoring Visits
- Source Documentation
- Excel
Qualifications
- Bachelor's Degree
- GCP Training
About McKesson
mckesson.comThe leading healthcare company for wholesale medical supplies & equipment, pharmaceutical distribution, and healthcare technology solutions.
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