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Clinical Research Coordinator

1+ years
$35.00 – $42.00 per hour
10 July 16, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Clinical Research Coordinator – Charleston, SC (Part-Time)

Location: Charleston, South Carolina
Job Type: Part-time (24 hours/week)
Compensation: $35.00 – $42.00 per hour
Work Mode: On-site


Job Summary

IQVIA is hiring a Clinical Research Coordinator to support clinical trials from its Charleston, SC site. This part-time, on-site role (24 hours/week) offers the opportunity to work in a hands-on clinical research setting, contributing to pediatric and adult trials. The ideal candidate will have experience in phlebotomy, pediatric care, and adherence to ICH-GCP guidelines. If you're looking to build a career in clinical operations, patient safety, and regulatory-compliant trial execution, this is the role for you.


Key Responsibilities

  • Perform complex procedures such as phlebotomy, spirometry, ECGs, and vital signs

  • Coordinate studies under the supervision of a Principal Investigator

  • Participate in community outreach and patient education

  • Review and interpret study protocols, CRFs, and electronic data systems

  • Conduct volunteer recruitment, screening, and orientation

  • Ensure the safety and rights of research volunteers

  • Administer study drugs per SOPs and monitor adverse events

  • Prepare and maintain study materials, supplies, and documentation

  • Ensure compliance with ICH-GCP and all regulatory standards

  • Assist with quality control and query resolution for clinical data

  • Act as a liaison with study monitors and sponsors during site visits


Required Skills & Qualifications

  • High School Diploma with minimum 1 year of clinical research experience

  • Prior experience in a clinical trials setting is preferred

  • Pediatric experience and phlebotomy skills required

  • Understanding of Good Clinical Practices (GCP) and trial protocol

  • Familiarity with medical terminology and research documentation

  • Relevant certifications/licenses as per regulatory requirements

  • Detail-oriented with excellent interpersonal and communication skills

  • Ability to manage multiple clinical tasks in a regulated environment


Perks & Benefits

  • Competitive hourly pay: $35.00–$42.00/hour

  • Work with a global CRO at the forefront of clinical research innovation

  • Opportunities for skill development in pediatric and community-based trials

  • Involvement in cutting-edge therapeutic studies and trial coordination

  • Exposure to global best practices and ICH-GCP standards


Company Description

IQVIA is a global leader in healthcare analytics and clinical research services, delivering transformative insights to life sciences organizations. Operating in over 100 countries, IQVIA empowers the development and delivery of innovative therapies that improve health outcomes and enhance population health.


Work Mode

On-site – Charleston, SC


Call to Action

Ready to contribute to groundbreaking clinical research? If you have pediatric or phlebotomy experience and a passion for trial coordination, apply now to join IQVIA as a Clinical Research Coordinator in Charleston, South Carolina.