×
Register Here to Apply for Jobs or Post Jobs. X

Clinical Research Nurse Coordinator, Duke Cancer Institute

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: Duke PF
Full Time position
Listed on 2025-12-31
Job specializations:
  • Science
    Clinical Research
Job Description & How to Apply Below

Select how often (in days) to receive an alert:

Clinical Research Nurse Coordinator, Duke Cancer Institute

Work Arrangement:

Requisition Number: 263512

Regular or Temporary:
Regular

Location:

Durham, NC, US, 27710

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.

You will provide leadership and coordination for multiple, complex oncology clinical trials—including investigational products (IP)—within the Duke Cancer Institute’s Brain Tumor Clinical Research Program (BTC). You’ll collaborate with the Oncology Clinical Research Unit (CRU), Principal Investigators (PIs), sponsors, and study teams to ensure feasibility, compliance, and participant-centered care. Daily, you will recruit and consent participants, conduct study visits, maintain regulatory documentation, and troubleshoot challenges to keep studies on track.

Your work spans operations, site management, communication, data integrity, leadership, and ethics. If you thrive in complex neuro-oncology research, enjoy mentoring others, and want to advance breakthrough therapies for brain tumor patients, this role is for you.

  • Education:

    Graduation from an accredited BSN or Associate Degree in Nursing or Nursing Diploma program. Registered nurses without a BSN must enroll within two years and complete within seven years of start date.
  • Licensure/

    Certifications:

    Current or compact RN licensure in North Carolina; BLS required; maintain active NCBON status and hospital/unit competencies.
  • Experience:

    Minimum of 12 months of appropriate clinical nursing experience.
Preferred Qualifications:
  • Oncology and/or clinical research experience.
  • Familiarity with EDC systems, investigational product handling, and Good Clinical Practice (GCP).
  • Experience coordinating multi-stakeholder studies and supporting site initiation/closeout.
Other Requirements:
  • On-call:
    Overnight and/or weekend call for Convection-Enhanced Delivery (CED) infusions.
  • Clinical competencies:
    Ambulatory medication administration, medication education and management, adult chemotherapy administration, basic dysrhythmia review, lab result review, adverse event assessment, and patient education.
  • Ability to interact effectively with multidisciplinary teams and support patient compliance.
  • Compliance:
    Maintain Duke and project-specific training and certification requirements; follow SOPs, regulations, and protocol requirements governing clinical research.
Be Bold.
  • Direct study operations for multiple complex neuro-oncology trials, including feasibility assessments, recruitment and retention strategies, informed consent, scheduling, and execution of participant visits.
  • Coordinate site management activities (initiation through closeout), maintain regulatory binders and study-level documentation, manage delegation of authority logs, record and report adverse events (AEs), and ensure compliance with institutional policies and SOPs.
  • Serve as the primary liaison among sponsors, PIs, CRU, monitors, and study personnel; communicate clearly and elevate issues appropriately to drive timely resolution.
  • Ensure high-quality data capture in EDC systems; recognize and troubleshoot data issues; uphold data security and provenance standards and support query resolution.
  • Partner with finance…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary