Clinical Trials Coordinator - Oncology Research

Sarah Cannon Research Institute; Nashville (TN); On-site; USD 52,000 - 75,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Study Coordinator to plan and monitor complex Phase I-IV clinical research protocols. You will work closely with physicians, data operations, sponsors, and study teams to ensure protocol adherence and data integrity.

Responsibilities include trial startup through close-out, patient eligibility verification, and safety reporting. The role requires a detail-oriented, independent worker with strong communication and Excel skills, based in

Qualifications

• Understanding of clinical trial data.
• Knowledge of FDA guidelines and GCP.
• Ability to work independently in a fast-paced environment.
• Detail-oriented and meticulous.
• Strong computer skills with trial databases and Excel.

Responsibilities

• Lead the execution of trials for the research team.
• Plan and track all assigned clinical activity across startup, interim, and close-out.
• Verify patient eligibility and discuss discrepancies with nursing staff and physicians.
• Monitor adherence to the protocol and report safety events.
• Coordinate with sponsors, investigators, and study teams; prepare reports.

Skills

Clinical trials data

FDA guidelines

GCP

Independent work

Interpersonal skills

Excel

Education

Bachelor Degree

Tools

MS Access

MS Excel

EDC systems

Job description

Sarah Cannon Research Institute (SCRI) is seeking a Study Coordinator to plan and monitor complex Phase I-IV clinical research protocols. You will work closely with physicians, data operations, sponsors, and study teams to ensure protocol adherence and data integrity.

Responsibilities include trial startup through close-out, patient eligibility verification, and safety reporting. The role requires a detail-oriented, independent worker with strong communication and Excel skills, based in