Clinical Research Nurse Coordinator

Responsibilities Coordinate and manage oncology clinical trials by recruiting, screening, consenting, and enrolling participants while ensuring adherence to study protocols and regulatory requirements Deliver direct patient care in a research setting, including medication administration, chemotherapy delivery, patient education, and monitoring for adverse events and treatment compliance Oversee study operations and compliance, maintaining regulatory documentation, reporting adverse events, supporting audits, and ensuring alignment with institutional policies, SOPs, and federal guidelines Collaborate with investigators, sponsors, and cross-functional teams to execute study activities, resolve issues, support monitoring visits, and contribute to study start‑up and closeout processes Support financial and data management efforts, including budget development, tracking study milestones, entering and validating clinical data, and ensuring data accuracy, security, and completeness Requirements Graduation from an accredited BSN program, Associate Degree in Nursing, or Nursing Diploma program Current or compact RN licensure in the state of North Carolina BLS certification required Minimum 12 months of clinical nursing experience If not BSN-prepared, must enroll in a BSN program within two years and complete within seven years Maintain compliance with all hospital and unit-specific competencies and training requirements #J-18808-Ljbffr Duke Careers