CLINICAL RESEARCH NURSE COORDINATOR

Be You.

The Duke Office of Clinical Research is looking for a Clinical Research Nurse Coordinator to join our team. You will participate in or lead the day-to-day operations of clinical research studies conducted by principal investigators at Duke Medicine. Your role will involve a variety of duties including the collection, compilation, documentation, and analysis of clinical research data. You may also oversee the work of junior staff.

Minimum Requirements:

• Graduation from an accredited BSN or Associate's Degree in Nursing or Nursing Diploma program.

• All registered nurses without a Bachelor's degree in Nursing (or higher) will be required to enroll in an appropriate BSN program within two years of their start date and to complete the program within seven years of their start date.

• Current or compact RN licensure in the state of North Carolina.
• BLS certification.
• Twelve months of appropriate clinical experience.

Preferred Qualifications:

• Experience in clinical research operations, including screening, scheduling, consenting, and collecting adverse event information.
• Familiarity with intellectual property rights, inventions patents, and technologies.
• Experience with data management and informatics, including the use of Electronic Data Capture (EDC) systems.

Other Requirements:

• Maintain compliance with required hospital and unit-specific training competencies.
• Active RN status with the North Carolina Board of Nursing (NCBON).

This position is: Onsite. The work is performed on-site or at a designated assignment location.

Be Bold.

• Clinical Research Operations: Screen, schedule, consent, and collect adverse event information for participants. Maintain subject-level documentation and prepare for research visits.

• Ethical and Participant Safety Considerations: Ensure the ethical conduct of research and the safety of research participants, especially vulnerable populations.
• Data Management and Informatics: Use and train others in EDC systems, enter data accurately, and ensure data security and provenance.
• Leadership and Professionalism: Encourage and support colleagues, participate in or lead committees, and mentor junior staff.
• Study and Site Management: Participate in sponsor-required training, develop protocol-specific systems, and ensure compliance with institutional requirements.

Choose Duke.

Join a team that values your contributions and supports your professional growth. At Duke, you will have the opportunity to work on meaningful projects that advance clinical research and improve patient care. Enjoy a collaborative work environment and access to continuing education opportunities.