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 and GCP, organize research information, observe subjects and assist with data analysis and reporting, schedule data collection, review and report adverse events and protocol deviations, monitor data quality and regulatory compliance, perform administrative duties related to the study, participate in protocol development activities, ensure timely delivery of study information and supplies from sponsors, educate potential participants and caregivers on protocol specifics, conduct safety and efficacy assessments per protocol (vital signs, EKGs, blood draws), assist the Clinical Trial Manager with oversight of vendors, recruitment, quality, and trial outcomes, and support staff development; requires high school diploma or equivalent with preferred Bachelor’s degree, CCRC certification preferred, and 2-3 years in medical field; indoor office work with potential overnight travel; equal opportunity employer.
Required Qualifications
- High school graduate or equivalent
- 2-3 years of experience in the medical field
- Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials
- Strong leadership and mentorship skills
- Ability to communicate effectively, both verbally and in writing
- Works independently and as part of a team
- CCRC certification preferred
- Bachelors Degree preferred
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