Clinical Research Coordinator — Onsite at Duke

Duke PA; Durham (NC); On-site; USD 61,000 - 102,000; Full time

Job summary

Duke PA in Durham, NC, seeks a Clinical Research Coordinator to support the Department of Anesthesiology's clinical studies. You will lead day-to-day operations, recruit participants, manage data, and ensure regulatory compliance under investigators and sponsors.

The role requires strong organizational skills, experience in regulatory submissions and data management, and the ability to work independently within a multidisciplinary team at Duke's academic medical center.

Qualifications

• Associate's degree required; minimum two years of clinical research experience.
• Experience coordinating studies with research participants and regulatory submissions.
• Knowledge of GCP, IRB processes, and study documentation best practices.

Responsibilities

• Coordinate and conduct study visits per approved protocols.
• Recruit, screen, enroll, and retain research participants.
• Maintain regulatory and study documentation; prepare submissions.
• Manage investigational products and study specimens.
• Support monitoring visits, audits, and inspections.

Skills

Clinical research

GCP / IRB

Regulatory submissions

Documentation management

Regulatory compliance

Education

Associate's degree

DOCR North Carolina State-Approved Clinical Research Apprenticeship Program

Tools

Microsoft Office

Job description

Duke PA in Durham, NC, seeks a Clinical Research Coordinator to support the Department of Anesthesiology's clinical studies. You will lead day-to-day operations, recruit participants, manage data, and ensure regulatory compliance under investigators and sponsors.

The role requires strong organizational skills, experience in regulatory submissions and data management, and the ability to work independently within a multidisciplinary team at Duke's academic medical center.