What are the responsibilities and job description for the Clinical Research Coordinator position at Barrington James?
Clinical Research Coordinator
Fort Lauderdale, FL area (covers 4 sites)
About the role
CRC covering four active research sites across the greater Fort Lauderdale area. This is a multi-site position — you'll split time between locations on a set rotation and need reliable transportation.
What you'll do
- Manage day-to-day study coordination across all four sites
- Conduct informed consent and patient visits per protocol
- Maintain source documents and complete data entry (EDC/CRF)
- Track and process lab specimens, drug accountability, and regulatory documents
- Communicate with sponsors, monitors, and PIs at each site
- Coordinate scheduling to keep visit windows on track across locations
What you need
- Patient facing experience or Clinical Research Coordinator experience.
- Comfort working across multiple sites with independent scheduling
- Working knowledge of GCP and ICH guidelines (Desired, not required)
- Strong documentation and organizational skills
- Reliable transportation (daily travel between sites required)
- CCRC/CCRP certification a plus, not required
Apply now if you're interested in gaining clinical research experience in multiple therapeutic areas.
Feel free to email me directly at jdmandarin@barringtonjames.com