Clinical Research Nurse Coordinator

UNC-Chapel Hill • Chapel Hill, NC

4d • Onsite

About The Position

This position will serve as a Clinical Research Nurse Coordinator within the department of Global Health and Infectious Diseases. This position independently coordinates and implements complex HIV-related clinical trials, including prevention, treatment, and cure-focused protocols. The Nurse Coordinator ensures protocol integrity, participant safety, regulatory compliance, and high-quality data collection while contributing to the unit’s research and clinical mission. This position has broad responsibility for the implementation of complex clinical trials. These trials include prevention, treatment and possible cure of HIV, as well as sexually transmitted diseases. This includes novel treatment approaches for people with HIV, such as testing community-based delivery of HIV treatment. The Nurse Consultant will utilize a broad knowledge of adult assessment and common health problems, HIV and other infectious diseases, medical ethics, Good Clinical Practice (GCP), as well as sponsor and study specific procedures and data collection. This position is a professional member of the staff and as such is expected to work independently, adhere to all University, Program and profession specific regulations as well as participate in unit wide activities and exhibit a high degree of accountability for all work. The Clinical Research Nurse Coordinator is responsible for independently providing specialized nursing services for various clinical research protocols. They are responsible for providing guidance and assistance to study teams in both clinical and non-clinical areas of research, including participant visits, data quality, and others.

Requirements

• Broad knowledge of adult assessment and common health problems.
• Knowledge of HIV and other infectious diseases.
• Knowledge of medical ethics.
• Knowledge of Good Clinical Practice (GCP).
• Knowledge of sponsor and study specific procedures and data collection.
• Ability to work independently.
• Adherence to all University, Program and profession specific regulations.
• High degree of accountability for all work.

Responsibilities

• Independently coordinates and implements complex HIV-related clinical trials, including prevention, treatment, and cure-focused protocols.
• Ensures protocol integrity, participant safety, regulatory compliance, and high-quality data collection.
• Contributes to the unit’s research and clinical mission.
• Provides specialized nursing services for various clinical research protocols.
• Provides guidance and assistance to study teams in both clinical and non-clinical areas of research, including participant visits and data quality.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: No Education Listed