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Site Research Assistant - San Dimas, Ca

Iqvia
IQVIA
1+ years
$25.00-$39.00 per hour
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

Site Research Assistant – San Dimas, CA
Location: San Dimas, California
Job Type: Part-Time (24 hours/week) | On-Site
Requisition ID: R1493027
Company: IQVIA

Salary:
$25.00 – $39.00 per hour
(Compensation may vary based on education, experience, skills, and location. Incentives, bonuses, and comprehensive benefits may also be offered.)


Position Overview:
IQVIA is hiring a Research Assistant to support clinical trial activities at the San Dimas, CA site. This is a fully on-site role ideal for professionals with at least 1 year of clinical research experience who are looking to build strong team relationships and contribute meaningfully to advancing healthcare research.


Key Responsibilities:

  • Perform EDC data entry and query resolution

  • Build strong rapport with investigators, site staff, and study team

  • Assist with screening, recruitment, and enrollment of study participants

  • Schedule study visits and coordinate follow-up care

  • Collect patient history and support documentation

  • Adhere to IRB-approved protocols and informed consent processes

  • Support patient safety monitoring

  • Coordinate all protocol-related research activities, study visits, and lab procedures

  • Ensure compliance with company and sponsor SOPs and regulatory guidelines

  • Maintain effective communication across research and clinical teams


Required Qualifications:

  • High School Diploma with 1+ year of clinical research experience

  • Familiarity with clinical trial operations and GCP principles

  • Strong understanding of medical terminology

  • Proficiency in Microsoft Office (Word, Excel, Outlook)

  • Detail-oriented with strong interpersonal skills

  • Ability to perform clinical procedures as required

  • Must have applicable certifications and licenses as required by regulatory bodies

  • Sponsorship is not available for this role