Clinical Research Coordinator (Greenville, SC)

Carolina Nephrology; Greenville (SC); On-site; USD 48,000 - 75,000; Full time

Benefits offered by this job

Travel reimbursement

Competitive compensation

Job summary

Carolina Nephrology Clinical Research in Greenville, SC is seeking a hands-on Clinical Research Coordinator to join our growing team. You’ll oversee day-to-day trial operations, coordinate studies from initiation to close-out, and ensure adherence to GCP, FDA, and IRB guidelines while collaborating with physicians, sponsors, and auditors.

The role offers opportunities to work on groundbreaking trials, travel between satellite offices, and participate in protocol development, data management, and

Qualifications

• 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.

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.

Skills

Organizational skills

Communication skills

Clinical research coordination

Attention to detail

Travel willingness

GCP/FDA regulations knowledge

Education

Bachelor's degree in healthcare or life sciences

Job description

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

Carolina Nephrology Clinical Research is an equal opportunity employer.