Clinical Research Coordinator (Greenville, SC)

Carolina-Nephrology,-P

Greenville (SC)

Presencial

USD 42.000 - 62.000

Jornada completa

Hace 6 días
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Ventajas ofrecidas por este puesto de trabajo

Travel and mileage reimbursement
Competitive compensation
Growth opportunities

Descripción de la vacante

Carolina Nephrology Clinical Research in Greenville, SC is seeking a Clinical Research Coordinator to join our growing team. You will manage day-to-day study operations, screen and enroll participants, maintain regulatory documentation, and liaise with sponsors and monitors.

The role requires strong organizational and communication skills, familiarity with GCP/FDA, and willingness to travel between satellite offices. This is a full-time position with occasional extended hours.

Formación

  • Strong organizational, critical thinking, and communication skills.
  • Prior experience coordinating clinical research studies 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.

Responsabilidades

  • 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).
  • Collect, manage, and document clinical data and regulatory documentation.
  • Serve as liaison with sponsors, monitors, labs, and auditors.
  • Train research team members on procedures and documentation standards.
  • Support development of study protocols and reporting documents.
  • Stay updated with industry best practices in clinical research.
  • Travel to satellite offices and work outside standard hours as needed.

Conocimientos

Organizational skills
Critical thinking
Communication skills
Study coordination
Willingness to travel

Educación

Bachelor's degree in healthcare or life sciences

Descripción del empleo

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.

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