Clinical Research Coordinator - 243223 Job at Medix™, Fayetteville, NC

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  • Medix™
  • Fayetteville, NC

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,

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