Clinical Research Coordinator

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

Overview

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.

Ref: #568-Clinical