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Research Assistant, On-Site, Mesa, Az

2+ years
$29,400 – $73,400
10 Aug. 29, 2025
Job Description
Job Type: Full Time Education: Demonstrated interest in clinical research or healthcare field 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: Mesa, Arizona
Job Type: Full-Time
Work Set-Up: Fully On-Site (Office-Based)
Job ID: R1498564
Availability: Position available in additional locations
Company: IQVIA


Position Overview:

This is an excellent entry-level opportunity for individuals interested in launching a career in clinical research. Ideal for those with strong teamwork skills and a passion for patient care, this role offers hands-on exposure to clinical trials in a supportive environment. Clinical skills (e.g., drawing blood, EKGs, obtaining vitals) are helpful but not required.


Key Responsibilities:

Clinical Trial Support

  • Assist with screening, recruitment, and enrollment of research participants.

  • Schedule participant appointments for study visits and follow-up procedures.

  • Collect and document patient history and other source data.

  • Coordinate protocol-specific research activities and laboratory procedures.

  • Participate in informed consent discussions and ensure adherence to IRB-approved protocols.

  • Support participant safety and well-being throughout the trial.

Data & Compliance

  • Perform accurate data entry and maintain clinical trial management systems.

  • Comply with all applicable guidelines including GCP/ICH, sponsor policies, and Avacare SOPs.

  • Manage documentation, filing systems, and clinical records in accordance with regulatory standards.

Team Collaboration

  • Develop strong, respectful working relationships with investigators, site staff, and study team members.

  • Maintain clear and effective communication across clinical and administrative teams.


Qualifications:

Required:

  • Demonstrated interest in clinical research or healthcare field.

  • Strong interpersonal skills with attention to detail.

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

  • Ability to adapt quickly and prioritize tasks in a dynamic environment.

Preferred:

  • Knowledge of GCP/ICH regulatory guidelines.

  • Familiarity with medical terminology.

  • Prior clinical experience (e.g., taking vitals, phlebotomy, EKGs) is a plus, but not required.


Compensation & Benefits:

  • Annual Base Pay Range: $29,400 – $73,400
    (Final offer may vary depending on experience, education, skills, location, and work schedule.)

  • May include additional incentive plans, bonuses, and comprehensive health and welfare benefits.


About IQVIA:

IQVIA is a global leader in clinical research, healthcare intelligence, and advanced analytics. We empower life sciences organizations with technology and insights that improve patient outcomes and advance public health initiatives.
Learn more: https://jobs.iqvia.com


Equal Opportunity Employer:

IQVIA is an Equal Opportunity Employer and complies with all applicable employment laws. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected characteristic.
EEO Policy: https://jobs.iqvia.com/eoe


How to Apply:

Search for Job ID: R1498564 at https://jobs.iqvia.com or click Apply Now to begin your application.