Clinical Research Coordinator (Spartanburg, SC)

Carolina Nephrology • Spartanburg, SC

23h

About The Position

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 Spartanburg, 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.

Requirements

• 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

Nice To Haves

• GCP and IATA certifications

Responsibilities

• 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

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level