Senior Oncology Clinical Research Coordinator (RN)

American Oncology Network; Columbus (OH); On-site; USD 37,000 - 68,000; Full time

Job summary

American Oncology Network is seeking a Clinical Research Coordinator III (RN) to supervise research studies under a PI. You will perform protocol-aware procedures, ensure GCP compliance, manage regulatory documents, and support adverse event reporting at Zangmeister Cancer Center.

The role requires 2–5 years nursing experience, oncology preferred, and an unencumbered RN license. You will coordinate visits, consent discussions, data entry in EMR/EDC, and monitor budgets across sites.

Qualifications

• RN license required; oncology nursing experience preferred.
• Bachelor's or Associate degree in Nursing required.
• Experience with clinical research processes and documentation.

Responsibilities

• Understand protocol elements and execute study procedures per protocol.
• Regulatory compliance: IRB/IEC, SOPs, and GCP adherence.
• Collect, record and report accurate data per FDA guidelines.
• Monitor safety: AE/SAE reporting to sponsor and IRB/IEC.
• Oversee budgeting, invoicing and contract execution for studies.
• Coordinate visits, consent discussions and data entry in EMR/EDC.

Skills

Regulatory compliance

Clinical coordination

Data integrity

Communication

Remote work ability

Education

Bachelor/Associate in Nursing

RN License

Tools

EMR

EDC

CTMS

MS Office

Job description

American Oncology Network is seeking a Clinical Research Coordinator III (RN) to supervise research studies under a PI. You will perform protocol-aware procedures, ensure GCP compliance, manage regulatory documents, and support adverse event reporting at Zangmeister Cancer Center.

The role requires 2–5 years nursing experience, oncology preferred, and an unencumbered RN license. You will coordinate visits, consent discussions, data entry in EMR/EDC, and monitor budgets across sites.