Clinical Research Coordinator

Joulé

Augusta, GA

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JOB DETAILS
SALARY
$30–$35.17 Per Hour
SKILLS
Case Report Form (CRF), Certified Clinical Research Coordinator (CCRC), Clinical Practices/Protocols, Clinical Research, Clinical Support, Communication Skills, Data Entry, Documentation, Electrocardiogram, Electronic Data Capture (EDC), GCP (Good Clinical Practices), Healthcare, ICH Regulations, Informed Consent, Maintain Compliance, Organizational Skills, Patient Safety, Phlebotomy, Project/Program Management, Research Skills, Sample/Specimen Processing, Time Management, Volume Planning
LOCATION
Augusta, GA
POSTED
2 days ago

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.



Ref: #568-Clinical


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/