Job Title: Clinical Research Coordinator
Location: Asheville, NC 100% Onsite
Schedule: Monday–Friday
Type: C ontract- 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.
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.
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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