Clinical Research Nurse Coordinator - Duke Cancer Institute

Clinical Research Nurse Coordinator - Duke Cancer Institute

Work Arrangement:
On-Site

Requisition Number: 271135 Regular or Temporary:
Regular

Location:

Durham, NC, US, 27710 Personnel Area: MEDICAL CENTER Date:
Jun 16, 2026

School of Medicine:
Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe.

Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.

Be You. The Duke Cancer Institute's Gastrointestinal (GI) Clinical Research Program is seeking a Clinical Research Nurse Coordinator to support the successful execution of complex oncology clinical trials within the Oncology Clinical Research Unit (CRU). In this role, you will play a critical part in advancing cancer research by coordinating multiple studies involving investigational products while ensuring high-quality patient care and regulatory compliance.

In your day-to-day work, you will collaborate closely with Principal Investigators (PIs), sponsors, and interdisciplinary teams to recruit, enroll, and manage study participants. You will help patients navigate clinical trial participation, provide education on study medications and procedures, and ensure safety through careful monitoring and documentation. This position offers the opportunity to directly impact cutting-edge oncology research while combining clinical nursing expertise with research operations, data management, and leadership responsibilities.

Minimum Requirements:

Graduation from an accredited BSN, ADN, or Nursing Diploma program Current RN licensure in North Carolina (or compact state) BLS certification required Twelve months of appropriate clinical nursing experience Ability to maintain compliance with hospital and unit-specific training competencies and NCBON requirements Nurses without a BSN are encouraged to enroll within two years and complete within seven years (exception applies to hires before September 1, 2016)

Preferred Qualifications:

Oncology nursing experience Clinical research experience, particularly in oncology trials Experience working with investigational products and clinical trial protocols

Other Requirements:
Ability to maintain required certifications and training for clinical research and nursing practice Strong understanding of regulatory, compliance, and ethical requirements in clinical research Participation in ongoing continuing education and professional development

This position is onsite, with work performed at designated Duke clinical and research locations

Be Bold.

Position Responsibilities:

• Lead and coordinate complex oncology clinical trials, including study feasibility, recruitment, enrollment, and retention strategies
• Recruit, screen, consent, and manage study participants, ensuring adherence to protocol requirements and patient-centered care
• Conduct and document study visits, including clinical assessments, adverse event monitoring, and patient education on study medications and side effects
• Administer medications and chemotherapy, review laboratory results, and provide clinical interventions as guided by the Principal Investigator
• Maintain study compliance with institutional policies, regulatory requirements, and protocol standards, including accurate documentation in regulatory binders and systems of record
• Record and report adverse events (AE) and ensure timely escalation of study…