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.

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