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Site Research Assistant - West Jordan, Ut

1+ years
$25.00 – $39.00 per hour
10 Oct. 16, 2025
Job Description
Job Type: Part Time Education: B.Sc/M.Sc/M.Pharma/B.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

Position: Site Research Assistant

📍 Location: West Jordan, Utah (Office-based)
🕒 Employment Type: Part-Time
💼 Job ID: R1503639
📅 Scheduled Hours: 24 hours/week


About IQVIA

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, helping accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
🔗 Learn more: https://jobs.iqvia.com


Job Overview

The Site Research Assistant will assist in conducting clinical trial activities in compliance with applicable regulations. The role requires logical thinking, prioritization skills, adaptability, and strong interpersonal and team-building abilities.


Responsibilities

Clinical Trial Support

  • Enter data into Electronic Data Capture (EDC) systems and resolve queries.

  • Assist with screening, recruiting, and enrollment of research subjects.

  • Collect patient/research participant history.

  • Perform patient/research participant scheduling.

  • Coordinate follow-up care and laboratory procedures.

  • Support the informed consent process and ensure subject safety.

  • Adhere to IRB-approved protocols.

  • Coordinate protocol-related procedures, study visits, and follow-up care.

  • Schedule subject visits and procedures.

Relationship Management

  • Develop and maintain effective communication with study team members.

  • Build strong relationships with investigators and office staff to foster trust and collaboration.

Compliance

  • Comply with company and sponsor policies, SOPs, and guidelines.

  • Maintain knowledge of protocol-specific procedures, consent forms, and study schedules.


Qualifications

  • Minimum Associate’s Degree or equivalent education/experience.

  • At least 1 year experience in a clinical research setting preferred.

  • Working knowledge of clinical trials and Good Clinical Practices (GCP).

  • Skilled in performing required clinical procedures.

  • Knowledge of medical terminology.

  • Strong attention to detail and organizational skills.

  • Ability to maintain effective working relationships with coworkers, managers, patients, physicians, and clients.

  • Applicable certifications/licenses as required by company, state, or regulatory authorities.

⚠️ Note: This position is not eligible for sponsorship.


Compensation & Benefits

  • Base pay range: $25.00 – $39.00 per hour, depending on qualifications, experience, and schedule.

  • May include incentives, bonuses, and other benefits depending on position.


Equal Opportunity

IQVIA is an equal opportunity employer. All qualified applicants are considered regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected status.
🔗 Equal Opportunity Statement


📩 Apply Now: IQVIA Careers – Site Research Assistant