Clinical Research Coordinator - Clinical Research
$52,000–$60,320 year
On-site · Savannah, Georgia, United States
Job Summary
Coordinate all aspects of clinical trials from study initiation to completion under ICH/GCP guidelines and company protocols. Organize research information, observe subjects, collect data, review adverse events and protocol deviations, monitor data quality, perform regulatory duties, and assist with vendor oversight and staff development. Educate participants and caregivers on protocol details, and perform safety and efficacy assessments (vital signs, EKGs, blood draws, and related tasks). Overnight travel may be required; shift is typically Monday–Friday, with an emphasis on compliance, documentation, and collaboration with the Clinical Trial Manager and sponsors.
Required Qualifications
- High school graduate or equivalent; Bachelors Degree preferred
- CCRC certification preferred
- 2-3 years of experience in the medical field preferred
- Knowledge of Federal regulations protecting human subjects in research governing clinical trials
- Strong leadership and mentorship skills
- Ability to develop and maintain effective working relationships at all levels (sponsor and vendor)
- Crisis management and problem-solving skills; calm under emergent situations
- Ability to work independently as well as part of a team
- Effective verbal and written communication skills
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