What are the responsibilities and job description for the Clinical Research Coordinator (Spartanburg, SC) position at CAROLINA NEPHROLOGY, PA?
We're Hiring: Clinical Research Coordinator!
Location: Spartanburg, 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 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.
What You'll Do
Carolina Nephrology Clinical Research is an equal opportunity employer.
PI284028747
Location: Spartanburg, 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 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.
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
- 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
- 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
Carolina Nephrology Clinical Research is an equal opportunity employer.
PI284028747