Greenville Clinical Research Coordinator — Impactful Trials

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

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