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Research Assistant, On-Site, South Ogden, Utah

10+ years
USD 29,400 – USD 73,400
10 Nov. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Research Assistant (On-Site) – South Ogden, Utah

Location: South Ogden, Utah
Job ID: R1510627
Position Type: Full-Time | Office-Based
Additional Locations Available

Position Overview

IQVIA is seeking motivated and detail-oriented Research Assistants for a fully on-site role in South Ogden, Utah. This opportunity is ideal for entry-level candidates aiming to build a long-term career in clinical research. If you are passionate about patient care, highly organized, and enthusiastic about contributing to clinical trials that advance healthcare, this role offers hands-on industry exposure and career growth.

Clinical skills such as taking vitals, drawing blood, or performing EKGs are beneficial but not required.


Key Responsibilities

  • Support the execution of clinical trial activities in full compliance with regulatory standards and study protocols.

  • Build and maintain effective working relationships with investigators, clinic staff, and study teams.

  • Assist with participant screening, recruitment, and enrollment.

  • Schedule patient/research participant visits and coordinate protocol-related procedures.

  • Collect and document participant medical history.

  • Perform accurate data entry and data management tasks.

  • Assist with the informed consent process under supervision.

  • Maintain adherence to IRB-approved protocols, SOPs, and sponsor guidelines.

  • Coordinate laboratory procedures, follow-up assessments, and safety monitoring.

  • Support the overall research workflow and ensure high-quality documentation.


Required Knowledge, Skills, and Abilities

  • Understanding of GCP/ICH guidelines and regulatory requirements.

  • Knowledge of medical terminology preferred.

  • Clinical skills (vitals, phlebotomy, EKGs) are advantageous but not mandatory.

  • Strong interpersonal communication, problem-solving, and organizational skills.

  • High attention to detail and ability to work effectively in a fast-paced clinical setting.

  • Proficiency in MS Office applications (Outlook, Word, Excel, PowerPoint, SharePoint).

  • Ability to manage clinical documentation and trial master file systems.


Experience Level

  • Entry-Level

  • No previous clinical research experience required

  • Prior experience in a healthcare, medical office, or patient-care environment is beneficial


Compensation

Annual base pay range: USD 29,400 – USD 73,400
Actual pay will vary based on experience, skills, location, and schedule. Additional incentives, bonuses, and benefits may apply.


About IQVIA

IQVIA is a leading global provider of clinical research services, real-world insights, and healthcare intelligence. Through advanced analytics and technology, IQVIA supports the development and commercialization of innovative therapies that improve patient outcomes worldwide.


Apply Now

Begin your clinical research career with a global industry leader and contribute to meaningful advancements in healthcare.