Clinical Research Coordinator (Greenville, SC)

Our take on this role

About this role

Coordinate clinical research studies for Carolina Nephrology, from initiation through close-out, including participant enrollment and study records. The full-time role requires travel to satellite offices and work outside standard hours as needed.

What could you bring from clinical work?

• Nurses, OTs and PTs: Your experience collecting assessment data and documenting clinical findings could help you collect and document clinical study data.
• SLPs and social workers: Explaining procedures or services to support informed decisions may help you explain study participation and obtain informed consent.

Full job description from Carolina Nephrology, PA

Description
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
Requirements
What We're Looking For:
Strong organizational, critical thinking, and communication skills
Prior experience coordinating clinical research studies strongly preferred
Familiarity with ICH-GCP and FDA regulations
Excellent attention to detail and ability to multitask in a regulated environment
Willingness to travel locally between offices and work occasional early mornings/late evenings
GCP and IATA certifications preferred (or ability to obtain upon hire)
Bachelor's degree in healthcare, life sciences, or related field preferred
What You'll Get:
The opportunity to be part of cutting-edge research that directly impacts patient care
A supportive, collaborative team environment with growth potential
Competitive compensation and benefits
Travel and mileage reimbursement when visiting satellite locations
Ready to contribute to life-changing research? Apply now and help shape the future of kidney care.

Carolina Nephrology Clinical Research is an equal opportunity employer.