Job Title: Clinical Research Coordinator
Location: Augusta, GA, 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 Augusta GA 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.