Clinical Research Coordinator (Greenville, SC)

We're Hiring: Clinical Research Coordinator!

Location: Greenville, SC (with travel to satellite offices as needed)

Schedule: Full-Time | Must be flexible for occasional extended hours

Department: Carolina Nephrology Clinical Research

Are you passionate about advancing medicine and improving patient outcomes? Carolina Nephrology Clinical Research is seeking a Clinical Research Coordinator (CRC) to join our growing research team in Greenville, SC. This is your opportunity to play a hands-on role in groundbreaking clinical trials while working alongside an expert team in a dynamic, fast-paced environment.

Certified Medical Assistants (CMA) are welcome to apply!

Why This Role Matters:

As a CRC, you'll be the critical link between physicians, patients, sponsors, and regulatory bodies-ensuring that all clinical trial activities run smoothly, ethically, and according to protocol. You'll work closely with the Principal Investigator but carry major responsibility for day-to-day study operations.

What You'll Do:

• Coordinate multiple clinical research studies from initiation through close-out
• Screen, recruit, and enroll eligible participants; obtain informed consent
• Ensure compliance with federal, state, and institutional guidelines (GCP, IATA, FDA, IRB, etc.)
• Collect, manage, and document clinical data, adverse events, and protocol deviations
• Maintain case report forms, drug/device accountability, and regulatory documentation
• Serve as the key liaison with sponsors, monitors, labs, and auditors
• Train and guide research team members in proper procedures and documentation standards
• Support the development of study protocols, procedural manuals, and reporting documents
• Stay up to date with industry best practices and emerging clinical research trends
• Travel to satellite offices and work outside of standard hours as needed