Job Description
Clinical Research Coordinator (CRC)
Fayetteville, NC | Full-Time, Contract-to-Hire | On-Site
We’re seeking an experienced Clinical Research Coordinator to independently manage clinical trials from start-up through close-out. This is a great opportunity to join a fast-paced, patient-centered research environment with a collaborative and supportive team.
Key Responsibilities:
- Oversee all aspects of assigned clinical trials, including recruitment, consenting, enrollment, and follow-up
- Coordinate and conduct patient visits, including phlebotomy, vitals, and study procedures
- Maintain accurate documentation in EDC systems and ensure compliance with GCP, HIPAA, and study protocols
- Serve as primary contact for sponsors, monitors, and study teams
- Support regulatory reporting and ensure audit readiness in partnership with a dedicated regulatory team
- Collaborate closely with investigators and clinical staff to ensure study success
Qualifications:
- 2+ years of CRC experience in industry-sponsored trials
- Skilled in phlebotomy, vital signs, and working with electronic systems (e-consent, EDC)
- Strong communication, organization, and problem-solving skills
- Ability to work independently and adapt to a dynamic workload
- Bilingual (English/Spanish) a plus
- Must be local and willing to travel between Fayetteville and Sanford, NC.
Job Tags
Full time, Contract work, Local area,