Clinical Research Coordinator I – Oncology Trials

About the role

The Clinical Research Coordinator I will support phase I‑III oncology clinical trials within the Clinical Research Management Office of the Lombardi Comprehensive Cancer Center. This on‑campus position ensures trial integrity, patient safety, and compliance with regulatory standards.

Key responsibilities

• Coordinate assigned oncology trials throughout the lifecycle, including scheduling procedures, specimen collection, and patient visits.
• Obtain and document informed consent in accordance with protocol, institutional policies, and regulatory guidelines.
• Maintain accurate trial data in the Clinical Trials Management System (CTMS) and collaborate with Data Managers to resolve queries.
• Facilitate sponsor meetings, site initiation visits, and monitor serious adverse event reporting.
• Liaise with hospital staff, physicians, IRB, finance teams, and auditors to ensure compliance and smooth trial operations.

Required profile

• Bachelor’s degree in a scientific or health‑related field.
• Three to five years of experience in clinical research, preferably oncology.
• Ability to work independently, strong attention to detail, and effective prioritization of competing responsibilities.

Required skills

• Proficiency with Clinical Trials Management Systems (CTMS).
• Knowledge of Good Clinical Practice (GCP) guidelines and HIPAA regulations.