Clinical Research Coordinator

Asheville, North Carolina

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Type: Contract

Experience: 0

Category: Scientific & Clinical

Contractor Work Model: Onsite

Brand: Joulé

Shift: On-Site

Compensation Range: 25.00 - 35.17 Per Hour

Job ID: 342973

Date Posted: 01/13/2026

Shortcut: http://jobs.systemone.com/J7JFn2


Job Title: Clinical Research Coordinator
Location: Asheville, NC 100% Onsite
Schedule: Monday–Friday
Type: Contract- 6 months with the possibility of extension

A leading healthcare research organization is seeking a Clinical Research Coordinator to support trials in the Asheville area. This is a high-enrolling study requiring strong patient-facing skills, organizational abilities, and project management experience. If you have a background in clinical research and enjoy patient interaction, this is an excellent opportunity to contribute to impactful maternal health research. Apply today for immediate consideration. 


Responsibilities

  • Screen, consent, and enroll patients into the study.

  • Serve as a liaison between investigators, sponsors, and site staff.

  • Ensure protocol compliance and patient safety through accurate informed consent.

  • Collect, review, and enter study data into electronic case report forms (EDC).

  • Track and report adverse events, deviations, and study progress.

  • Maintain study documentation and create source tools as needed.

  • Support clinical procedures, such as ECGs, phlebotomy, and specimen processing/shipping.

  • Participate in sponsor meetings, monitoring visits, and site audits.


Requirements

  • Bachelor’s degree required.

  • 1+ years of clinical research experience (any therapeutic area).

  • Prior patient-facing role with informed consent experience.

  • Experience with research project management or high-volume study enrollment.

  • Strong organizational, communication, and time management skills.

  • Basic knowledge of ICH/GCP guidelines and clinical research regulations.

  • Phlebotomy or specimen-handling experience required.

  • Certified Clinical Research Coordinator (CCRC) credential a plus.



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