Clinical Research Nurse Coordinator

Duke Careers; Durham (NC); On-site; USD 70,000 - 90,000; Full time

Job summary

Jobtailor is seeking a registered nurse to coordinate oncology clinical trials in Durham, North Carolina. You will recruit, screen, consent, and enroll participants while ensuring adherence to study protocols and regulatory requirements in a hospital research setting.

The role includes direct patient care, medication administration, chemotherapy delivery, and monitoring for adverse events, with emphasis on compliance, data accuracy, and collaboration with investigators and sponsors.

Qualifications

• Graduation from an accredited nursing program (BSN/ADN or Diploma).
• Current RN licensure in North Carolina.
• BLS certification required.
• Minimum 12 months of clinical nursing experience.
• If not BSN-prepared, must enroll in BSN within two years and complete within seven years.
• Maintain compliance with hospital and unit competencies and training requirements.

Responsibilities

• Coordinate and manage oncology clinical trials by recruiting, screening, consenting, and enrolling participants.
• Deliver direct patient care in a research setting, including medication administration and chemotherapy delivery.
• Monitor adverse events and treatment compliance.
• Oversee study operations and regulatory documentation, reporting adverse events, supporting audits, and aligning with policies and federal guidelines.
• Collaborate with investigators and sponsors to execute study activities and support monitoring visits.
• Support budget tracking and data management, ensuring data accuracy and security.

Skills

Clinical nursing

Regulatory compliance

Team collaboration

Education

RN licensure (NC)

BSN/ADN/Nursing Diploma

BLS certification

Job description

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