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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 – Smyrna, GA (Part-Time)

Location: Smyrna, Georgia
Job Type: Part-time (20 hours/week)
Compensation: $35.00 – $42.00 per hour
Work Mode: On-site


Job Summary

IQVIA is seeking a detail-oriented Clinical Research Coordinator to support clinical trials from its on-site location in Smyrna, GA. This part-time position (20 hours per week) involves participant care, protocol coordination, phlebotomy, and pediatric patient interaction. The role is ideal for professionals experienced in Good Clinical Practices (GCP), patient safety, and regulatory compliance. Join a globally recognized healthcare leader to contribute meaningfully to clinical innovation and public health.


Key Responsibilities

  • Perform complex procedures including phlebotomy, spirometry, ECGs, and vital signs

  • Coordinate clinical trials per study protocol and regulatory guidelines

  • Participate in community outreach and pediatric research activities

  • Review and interpret study protocols, CRFs, and related documents

  • Assist in volunteer recruitment, screening, and orientation

  • Maintain high standards in volunteer safety, care, and study conduct

  • Support study setup including labeling, logistical planning, and training

  • Administer investigational products and record clinical data accurately

  • Adhere to ICH-GCP guidelines and ensure data accuracy and completeness

  • Work closely with investigators, study monitors, and research teams


Required Skills & Qualifications

  • High School Diploma with minimum 1 year clinical research experience

  • Working knowledge of GCP, clinical protocols, and trial operations

  • Phlebotomy experience and comfort with pediatric populations

  • Understanding of medical terminology and research documentation

  • Certifications/licenses as required by state or employer regulations

  • Strong attention to detail and communication skills

  • Ability to manage volunteer safety and regulatory compliance

  • Familiarity with study drug administration protocols


Perks & Benefits

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

  • Opportunity to work with leading global CRO – IQVIA

  • Enhance expertise in pediatric trials and protocol coordination

  • Engage in community outreach and volunteer engagement

  • Exposure to innovative clinical research practices and technology


Company Description

IQVIA is a world leader in clinical research and healthcare intelligence, supporting biopharma and life sciences companies in bringing new therapies to market faster and more efficiently. With operations in over 100 countries, IQVIA provides data-driven insights that improve patient outcomes and public health.


Work Mode

On-site – Smyrna, GA


Call to Action

If you have experience in clinical trial coordination, pediatric care, or phlebotomy, and want to make a meaningful impact in healthcare, apply now to join IQVIA as a Clinical Research Coordinator in Smyrna, GA.