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

• 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