Oncology Clinical Research Coordinator

Sarah Cannon Research Institute; Nashville (TN); On-site; USD 48,000 - 80,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is conducting clinical trials through a broad network across the country. The Clinical Research Coordinator supports overall clinical operations, enrollment, regulatory tasks, quality control, and site activities to ensure protocol compliance and patient safety.

Ideal candidates hold related degrees and knowledge of regulatory guidelines, with strong organization and communication skills to coordinate with physicians, monitors, and study teams.

Qualifications

• Associate degree preferred, Bachelor’s degree desired.
• Knowledge of medical and research terminology.
• Knowledge of FDA Code of Federal Regulations and GCP.
• Knowledge of clinical research processes.
• Public presentation skills.
• Ability to manage multiple priorities with a diverse team.

Responsibilities

• Enroll patients onto clinical trials through recruitment, screening, enrollment, treatment and follow-up.
• Review study design and inclusion/exclusion criteria with physicians and patients.
• Ensure protection of study patients by verifying informed consent procedures and adherence to protocols.
• Collect, enter data into study CRFs or EDC within required timelines.
• Ensure data integrity through source document review and monitoring for missing data.
• Create study-specific tools for source documentation when not provided by sponsor.
• Generate and track drug shipments, lab kits, and other supplies.
• Maintain complete documentation of protocol requirements per SOPs and work instructions.
• Track and report adverse events and protocol deviations.
• Maintain regulatory documents, consent forms, source documentation, and study communications.
• Coordinate regular site research meetings and attend study meetings as required.
• Communicate site status via weekly activity reports to management.

Skills

Medical terminology

Clinical research knowledge

Multitasking

Public speaking

FDA CFR & GCP awareness

Education

Associate’s Degree

Bachelor’s Degree

Tools

Electronic Data Capture (EDC) systems

Job description

Sarah Cannon Research Institute (SCRI) is conducting clinical trials through a broad network across the country. The Clinical Research Coordinator supports overall clinical operations, enrollment, regulatory tasks, quality control, and site activities to ensure protocol compliance and patient safety.

Ideal candidates hold related degrees and knowledge of regulatory guidelines, with strong organization and communication skills to coordinate with physicians, monitors, and study teams.