What are the responsibilities and job description for the Clinical Research Coordinator position at Medix™?
About the Opportunity
We are seeking motivated Clinical Research Coordinators (CRC I, II, or III) to join a rapidly growing private clinical research network. This is an excellent opportunity to work in a fast-paced, high-enrolling research environment while contributing to the advancement of new therapies across multiple therapeutic areas.
Whether you're an experienced coordinator or looking to continue growing your clinical research career, this role offers structured onboarding, career advancement, and the opportunity to manage studies from start-up through closeout.
Responsibilities
- Coordinate clinical trials from screening and enrollment through study completion.
- Recruit, consent, and enroll study participants.
- Conduct patient visits, obtain vitals, perform ECGs, and support study procedures.
- Maintain accurate source documentation and regulatory files.
- Enter and manage study data in EDC/eSource systems.
- Ensure compliance with GCP, IRB requirements, and study protocols.
- Track adverse events (AEs/SAEs) and protocol deviations.
- Communicate with physicians, sponsors, monitors, and research staff.
- Support study start-up, maintenance, and closeout activities.
- Manage multiple active enrolling studies while maintaining quality and compliance.
Salary : $56,000 - $62,400