Oncology Clinical Trials Coordinator

Sarah Cannon Research Institute; Nashville (TN); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Total Rewards package

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Study Coordinator to plan, monitor, and execute complex clinical research protocols in Phase I-IV. You will collaborate with the physician PI, data operations, sponsors, and study teams to ensure protocol adherence and data quality.

You will support data collection, safety monitoring, and reporting while maintaining source documentation and study tools. Strong organization, communication, and knowledge of GCP are essential.

Qualifications

• Understanding of clinical trial data and processes.
• Knowledge of FDA guidelines and GCP is required.
• Ability to work independently in a fast-paced environment.
• Interpersonal skills, detail-oriented and meticulous.
• Computer skills with clinical trial databases, EDC, MS Access and Excel.
• Bachelor degree preferred.
• At least 1 year of healthcare/research experience.
• At least 1 year of planning and managing clinical trial processes.

Responsibilities

• Lead execution of trials for the research team.
• Plan and track all assigned clinical activity through startup, interim and close out.
• Confirm patient eligibility and discuss discrepancies with nursing staff and physicians.
• Verify study procedures are performed within protocol-specified windows.
• Participate in sponsor teleconferences to update on patients and study data.
• Present in weekly protocol meetings to investigators, staff and management.
• Provide safety information to sponsor and teams by monitoring adverse events.
• Update study tools and documentation for amendments or changes.
• Collect and enter data into CRFs or EDC within agreed timeframes.
• Maintain study documentation and correspondence per policy.
• Provide required metrics to leadership and drive process improvements.

Skills

Clinical trial data

FDA guidelines

GCP

Independent work

Interpersonal skills

Detail-oriented

MS Access

Excel

Electronic data capture

Trial process planning

Education

Bachelor's degree preferred

Healthcare/research experience

Tools

MS Access

Excel

Electronic data capture systems

Job description

Sarah Cannon Research Institute (SCRI) is seeking a Study Coordinator to plan, monitor, and execute complex clinical research protocols in Phase I-IV. You will collaborate with the physician PI, data operations, sponsors, and study teams to ensure protocol adherence and data quality.

You will support data collection, safety monitoring, and reporting while maintaining source documentation and study tools. Strong organization, communication, and knowledge of GCP are essential.