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Research Assistant, On-Site, Phoenix, Arizona

0-2 years
$29,400 – $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) – Phoenix, Arizona

Location: Phoenix, Arizona
Job Type: Full-Time
Requisition ID: R1510125
Work Setting: Office-Based
Additional Locations Available


About the Role

This full-time, on-site Research Assistant position in Phoenix, Arizona offers an excellent opportunity for individuals looking to begin or advance their career in clinical research. This role is ideal for candidates who are passionate about patient care, possess strong communication skills, and are eager to contribute to the execution of clinical trials that support advancements in healthcare.

While previous clinical skills such as obtaining vitals, performing EKGs, or drawing blood are beneficial, they are not mandatory. Comprehensive training will be provided.


Key Responsibilities

  • Support the execution of clinical trial activities in compliance with GCP/ICH guidelines and regulatory requirements

  • Build effective working relationships with investigators, clinical staff, and study team members

  • Assist with screening, recruiting, and enrolling study participants

  • Schedule patient visits and manage participant follow-up

  • Collect medical histories and support data entry activities

  • Coordinate laboratory procedures and protocol-specific tasks

  • Participate in the informed consent process

  • Uphold patient safety and ensure adherence to approved study protocols

  • Support documentation, record keeping, and management of trial-related systems

  • Ensure compliance with internal SOPs and sponsor guidelines


Required Knowledge, Skills, and Abilities

  • Understanding of GCP/ICH guidelines and regulatory compliance

  • Knowledge of medical terminology preferred

  • Clinical exposure or skills preferred but not required

  • Strong interpersonal communication and attention to detail

  • Proficiency in MS Office applications including Word, Excel, PowerPoint, Outlook, SharePoint

  • Ability to adapt in a dynamic environment and prioritize tasks efficiently


Experience Level

  • Entry-Level to Early Career

  • Ideal for candidates with 0–2 years of clinical, healthcare, or patient-facing experience

  • Previous exposure to clinical research or patient care is beneficial but not required

  • Training will be provided for individuals new to clinical research


Compensation

Annual Base Pay Range:
$29,400 – $73,400, depending on qualifications, experience, and location.
Additional compensation may include performance incentives, bonuses, and a comprehensive benefits package based on role eligibility.


About IQVIA

IQVIA is a global leader in clinical research, healthcare analytics, and life sciences solutions. The organization delivers innovative insights and accelerates the development and commercialization of medical treatments to improve patient outcomes worldwide.


Equal Employment Opportunity

IQVIA is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected categories.


Apply Now to start your career in clinical research and contribute to impactful clinical studies that support the future of healthcare.