Full-time
Clinical Research Coordinator (Greenville, SC)
Competitive
CAROLINA NEPHROLOGY, PAScience & PharmaceuticalPosted 18d ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
18 days ago
Job description
Carolina Nephrology Clinical Research is seeking a Clinical Research Coordinator to manage day-to-day clinical trial operations. The role coordinates studies from initiation through close-out, supports participants and research teams, and ensures accurate documentation and regulatory compliance.
Tags
Hospital & Health Care
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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
Preferred
Prior experience coordinating clinical research studies strongly preferred
GCP and IATA certifications preferred
Bachelor's degree in healthcare, life sciences, or related field preferred
Benefits
The opportunity to be part of cutting-edge research that directly impacts patient care
A supportive, collaborative team environment with growth potential
Travel and mileage reimbursement when visiting satellite locations
CAROLINA NEPHROLOGY, PA is a medical practice specializing in kidney care based out of 203 MILLS AVENUE, GREENVILLE, South Carolina.
GREENVILLE, South Carolina, US
https://www.carolinanephrology.com/
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Qualifications
Strong organizational, critical thinking, and communication skills
Familiarity with ICH-GCP and FDA regulations
Excellent attention to detail and ability to multitask in a regulated environment
Prior experience coordinating clinical research studies strongly preferred
GCP and IATA certifications preferred
Bachelor's degree in healthcare, life sciences, or related field preferred
Required skills
Clinical Research Coordination, ICH-GCP, FDA Regulations, IATA Certification
Preferred skills
GCP and IATA certifications preferred
Experience
Mid level
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