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Research Assistant

1 years
$25.00 – $39.00
10 Sept. 8, 2025
Job Description
Job Type: Part Time Education: B.Sc/M.Sc/ B.Pharma/ M.Pharma/ Life Sciences 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

Job Title:

Research Assistant


Location:

West Jordan, Utah
On-site / Office-based


Work Schedule:

  • Part-time

  • Scheduled Weekly Hours: 24

  • Work Set-Up: On-site


Job ID:

R1503639


Compensation:

  • Hourly Pay Range: $25.00 – $39.00

  • Actual pay may vary based on:

    • Knowledge, skills, education, and experience

    • Location

    • Full-time vs. part-time status

  • May be eligible for:

    • Incentive plans

    • Bonuses

    • Health and welfare benefits


About the Role:

As a Research Assistant, you will play a vital role in supporting the execution of clinical trials in compliance with regulatory standards. This includes tasks related to data entry, patient interaction, study coordination, and communication with internal and external stakeholders.


Key Responsibilities:

Clinical & Patient Support

  • Assist in screening, recruiting, and enrolling research subjects

  • Support informed consent process

  • Schedule subject visits and study procedures

  • Perform participant scheduling and collect patient histories

  • Coordinate follow-up care and lab procedures

  • Ensure adherence to IRB-approved protocols

  • Monitor patient safety and protocol compliance

Data Management & Coordination

  • Enter data into EDC (Electronic Data Capture) systems

  • Resolve queries in EDC

  • Maintain effective communication with study team members

  • Coordinate protocol-related procedures and study visits

Compliance & Communication

  • Follow GCP (Good Clinical Practice) guidelines

  • Comply with SOPs, sponsor requirements, and company policies

  • Build strong working relationships with investigators and office staff


Qualifications:

Required:

  • Associate’s degree (or equivalent education and experience)

  • Working knowledge of clinical trials and GCP

  • Strong interpersonal and communication skills

  • Attention to detail

  • Familiarity with medical terminology

  • Ability to perform clinical procedures

Preferred:

  • At least 1 year of experience in a clinical research setting

  • Experience with protocol guidelines and study schedules

Licenses/Certifications:

  • Must meet any applicable certifications and licenses required by company, state, or regulatory bodies


Additional Notes:

  • No sponsorship available for this position

  • Applicable tags:
    #LI-CES #LI-DNP #LI-HCP #ONSITE


Company Overview:

IQVIA is a global leader in clinical research services, healthcare data analytics, and life sciences consulting. They provide insights and technology solutions to help improve patient outcomes and accelerate the development of medical innovations.

Learn more: https://jobs.iqvia.com
EEO Statement: https://jobs.iqvia.com/eoe


How to Apply:

Apply Now