What are the responsibilities and job description for the Clinical Research Coordinator position at System One?
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
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Screen, consent, and enroll patients into the study.
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Ensure protocol compliance and patient safety through accurate informed consent.
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Collect, review, and enter study data into electronic case report forms (EDC).
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Maintain study documentation and create source tools as needed.
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Support clinical procedures, such as ECGs, phlebotomy, and specimen processing/shipping.
Requirements
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Bachelor’s degree required.
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1 years of clinical research experience (any therapeutic area).
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Prior patient-facing role with informed consent experience.
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Experience with research project management or high-volume study enrollment.
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Phlebotomy or specimen-handling experience required.
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Certified Clinical Research Coordinator (CCRC) credential a plus.
Ref: #568-Clinical