Oncology Study Coordinator – Hybrid in Nashville

McKesson; Nashville (TN); Hybrid; USD 55,000 - 75,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is hiring a Study Coordinator in Nashville. The role focuses on planning and monitoring complex clinical trials (Phase I–IV), data management, and collaboration with physicians, sponsors, and study teams.

You will ensure adherence to protocol timelines and prepare reports for leadership. The candidate should understand clinical trial data, know FDA guidelines and GCP, and be able to work independently in a fast-paced environment.

Qualifications

• Understanding of clinical trial data and regulatory guidelines.
• Ability to work independently in a fast-paced environment.
• Experience with data capture and trial management processes.

Responsibilities

• Plan and monitor startup, interim and close-out phases for trials.
• Verify patient eligibility and adherence to protocol windows.
• Collect and enter data into CRFs or EDC systems within timelines.
• Prepare reports and participate in sponsor/monitor communications.
• Support audit activities and respond to findings.
• Maintain study documents and tracking databases.

Skills

Clinical trial data understanding

FDA guidelines & GCP

Independent work style

Interpersonal skills

MS Excel / trial databases

Education

Bachelor degree preferred

Tools

MS Access

MS Excel

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is hiring a Study Coordinator in Nashville. The role focuses on planning and monitoring complex clinical trials (Phase I–IV), data management, and collaboration with physicians, sponsors, and study teams.

You will ensure adherence to protocol timelines and prepare reports for leadership. The candidate should understand clinical trial data, know FDA guidelines and GCP, and be able to work independently in a fast-paced environment.