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Site Research Assistant -Johns Creek, Ga

1+ years
$25.00 – $39.00 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

 

Site Research Assistant – Johns Creek, GA (Part-time)

Location: Johns Creek, GA (Office-based)
Job Type: Part-time (24 hours/week)
Salary Range: $25.00 – $39.00 per hour
Work Mode: On-site


Job Summary

IQVIA is seeking a Site Research Assistant to join its clinical site team in Johns Creek, Georgia. This part-time on-site position plays a vital role in supporting clinical trial operations and patient engagement. You will assist with data entry, subject screening, informed consent, and coordination of trial visits, while adhering to Good Clinical Practice (GCP) guidelines and sponsor protocols.

This is a great opportunity for professionals seeking entry-level clinical research roles or experienced assistants looking to deepen their experience within a global CRO.


Key Responsibilities

  • Perform Electronic Data Capture (EDC) entry and resolve queries

  • Assist in screening, recruiting, and enrolling clinical research subjects

  • Schedule participant visits and procedures in accordance with protocol timelines

  • Coordinate follow-up care and collect participant medical history

  • Support the informed consent process and ensure adherence to IRB-approved protocols

  • Maintain strong working relationships with site staff, physicians, and research teams

  • Comply with GCP, SOPs, and regulatory guidelines during all research activities

  • Track and support the safety and well-being of study participants

  • Maintain accurate documentation for all study-related tasks


Required Skills & Qualifications

  • High school diploma or equivalent with 1+ year of experience in clinical research

  • Strong working knowledge of Good Clinical Practice (GCP) and clinical trial processes

  • Familiarity with informed consent, study protocols, and trial visit schedules

  • Excellent communication and interpersonal skills to engage with staff and participants

  • Detail-oriented and organized, with strong time management capabilities

  • Ability to perform required clinical procedures and understand medical terminology

  • Certifications as required by local or federal regulations


Perks & Benefits

  • Hourly pay between $25.00 – $39.00, based on experience and qualifications

  • Opportunity to contribute to cutting-edge pharmaceutical research

  • Gain hands-on experience in site-based clinical trial operations

  • Join a globally recognized leader in clinical research and healthcare intelligence

  • Supportive team environment with room for learning and growth


Company Description

IQVIA is a global leader in clinical research and healthcare data analytics, providing intelligent solutions to life sciences and pharmaceutical companies. Our services help accelerate innovation, improve trial outcomes, and transform the delivery of care around the world.


Work Mode

On-site – Johns Creek, GA


Call to Action

Are you ready to make a meaningful impact in clinical research? Apply now to join IQVIA as a Site Research Assistant and be part of advancing healthcare through science and data.