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Site Research Assistant

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 – Hammond, LA (Part-time)

Location: Hammond, Louisiana
Job Type: Part-time (24 hours/week)
Compensation: $25.00 – $39.00 per hour
Work Mode: On-site


Job Summary

IQVIA is hiring a Site Research Assistant in Hammond, LA, for a part-time, on-site role supporting clinical research operations. The ideal candidate will contribute to the efficient conduct of clinical trials, with key responsibilities in EDC data entry, subject scheduling, and participant coordination. This is a valuable opportunity for professionals with a background in clinical research, GCP compliance, or patient care coordination to join a globally recognized leader in life sciences.


Key Responsibilities

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

  • Build and maintain professional relationships with study teams and investigators

  • Assist in subject screening, recruitment, and enrollment

  • Schedule research participants and manage follow-up visits

  • Collect patient histories and coordinate laboratory procedures

  • Participate in informed consent and uphold IRB-approved protocols

  • Support protocol-compliant clinical procedures and subject safety

  • Adhere to SOPs, sponsor guidelines, and regulatory requirements

  • Manage calendar for subject visits and protocol-specific activities


Required Skills & Qualifications

  • High School Diploma with at least 1 year of experience in clinical research

  • Knowledge of clinical trial processes and GCP principles

  • Familiarity with study protocols, SOPs, and consent forms

  • Ability to carry out protocol-mandated clinical procedures

  • Strong attention to detail and ability to multitask

  • Excellent communication and interpersonal skills

  • Proficient in medical terminology and clinical documentation

  • Certifications/licenses as per local regulations (if applicable)

  • Not eligible for sponsorship (must be authorized to work in the U.S.)


Perks & Benefits

  • Competitive pay range: $25.00 – $39.00 per hour

  • Opportunity to work on impactful clinical trial projects

  • Collaborate with leading investigators and clinical teams

  • Gain exposure to regulated healthcare and research standards

  • Work with a global healthcare leader and expand your career in clinical operations


Company Description

IQVIA is a global leader in clinical research and healthcare data analytics, empowering life sciences organizations to innovate, improve patient outcomes, and deliver transformative therapies. With world-class technology and domain expertise, IQVIA supports the advancement of modern healthcare worldwide.


Work Mode

On-site – Hammond, LA


Call to Action

Eager to be part of a world-class clinical research team? Apply now to become a Site Research Assistant at IQVIA and help shape the future of healthcare innovation from Hammond, Louisiana.