Clinical Research Coordinator – Oncology Trials

About the role

The Clinical Research Coordinator 1 will support phase I‑III oncology clinical trials within the Lombardi Comprehensive Cancer Center at Georgetown University. This full‑time position works closely with investigators, study participants, and the Clinical Trials Office to ensure trial integrity and patient safety.

Key responsibilities

• Coordinate assigned clinical trials throughout the entire lifecycle, from recruitment to close‑out.
• Screen and enroll participants, obtain informed consent, and document eligibility per protocol.
• Conduct study‑related procedures, manage specimen collection, and maintain protocol compliance.
• Provide patient education on trial participation, treatment expectations, and side‑effect management.
• Update the Clinical Trials Management System (CTMS) with accurate patient data and key dates.
• Collaborate with data coordinators to resolve queries and ensure complete documentation.
• Report serious adverse events and act as liaison with IRB, hospital staff, finance teams, and auditors.

Required profile

• Knowledge of Human Subject Protection regulations, HIPAA, and Good Clinical Practice.
• Ability to communicate effectively with investigators, participants, and multidisciplinary teams.
• Strong organizational skills to manage multiple trials simultaneously.
• Commitment to maintaining patient confidentiality and trial integrity.

Required skills

• Good Clinical Practice (GCP) compliance
• HIPAA compliance
• Clinical Trials Management System (CTMS) usage
• Human Subject Protection regulations