Clinical Research Coordinator – Oncology Trials

About the role

The Clinical Research Coordinator 1 will support phase I, II, and III oncology clinical trials at the Lombardi Comprehensive Cancer Center. This position ensures trial integrity, patient safety, and compliance with all regulatory requirements.

Key responsibilities

• Coordinate assigned clinical trials throughout the entire lifecycle, from start‑up to close‑out.
• Recruit, screen, and enroll study participants, obtaining informed consent in line with protocol and institutional policies.
• Conduct study‑related procedures, manage specimen collection, and maintain accurate documentation in the Clinical Trials Management System (CTMS).
• Provide patient education on trial participation, treatment expectations, and potential side effects.
• Collaborate with investigators, data managers, IRB, and finance teams to ensure complete and accurate trial records.
• Report serious adverse events and act as liaison with hospital staff, auditors, and review committees.

Required profile

• Experience coordinating oncology clinical trials (phase I‑III) in an academic medical center.
• Knowledge of Human Subject Protection regulations, HIPAA, and Good Clinical Practice (GCP).
• Strong organizational skills and ability to manage multiple tasks across inpatient, outpatient, and home settings.

Required skills

• Proficiency with Clinical Trials Management Systems (CTMS).
• Understanding of GCP guidelines.
• Familiarity with HIPAA compliance and IRB processes.

What we offer

• Opportunity to work with leading oncology investigators in a premier cancer center.
• Professional development through in‑service training and collaborative research environment.