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Research Assistant, On-Site, Lakewood, Colorado

2+ years
$29,400 – $73,400 annually
10 Aug. 5, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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
Location: Lakewood, Colorado
Job Type: Full-Time | Office-Based
Requisition ID: R1493674
Company: IQVIA

Salary:
$29,400 – $73,400 annually
(Compensation may vary based on qualifications, skills, experience, and location. Benefits and incentives may be offered in addition.)


Position Overview:
IQVIA is actively hiring a full-time Research Assistant for its Lakewood, Colorado site. This fully on-site role is ideal for entry-level professionals looking to launch a career in clinical research. If you enjoy patient care, are detail-oriented, and eager to be a part of life-changing clinical trials, this opportunity is for you. No prior clinical experience is required, though skills like drawing blood, taking vitals, or performing EKGs are a plus.


Key Responsibilities:

  • Build strong working relationships with investigators, site staff, and clinical study teams

  • Assist in subject screening, recruiting, and enrollment for trials

  • Coordinate subject visit scheduling and research procedures

  • Perform data entry and help manage participant records

  • Collect patient histories and support follow-up care and lab coordination

  • Assist in the informed consent process and ensure IRB protocol compliance

  • Adhere to sponsor and company SOPs, GCP/ICH guidelines, and regulatory protocols

  • Support participant safety and help maintain trial documentation


Preferred Skills & Qualifications:

  • Knowledge of GCP/ICH regulations

  • Familiarity with medical terminology preferred

  • Strong interpersonal skills and high attention to detail

  • Proficiency in Microsoft Office tools (Word, Excel, PowerPoint, Outlook, SharePoint)

  • Previous experience in clinical settings or research roles is beneficial but not required