Site Research Assistant - Lake Forest, Ca

Iqvia

1 year years

Not Disclosed

California

10 Aug. 29, 2025

Job Description

Job Type: Full Time Education: Minimum Associate’s degree or equivalent education and experience. 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: Site Research Assistant

Location: Lake Forest, CA / Mission Viejo, CA
Job Type: Part-Time (32 hours/week)
Work Set-Up: On-site (Office-based)
Job ID: R1501959
Availability: Also available in additional locations
Compensation: $25.00 - $39.00 per hour (dependent on qualifications, location, schedule, etc.)

Company Overview:

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. The company connects data, technology, and expertise to accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and public health.
Learn more: https://jobs.iqvia.com

Position Summary:

As a Research Assistant, you will assist in the execution of clinical trial activities in compliance with applicable regulations. Success in this role requires logical thinking, adaptability, strong prioritization, interpersonal, and teamwork skills.

Key Responsibilities:

Clinical Trial Support:

Perform Electronic Data Capture (EDC) entry and resolve data queries.
Assist with subject screening, recruitment, enrollment, and informed consent process.
Coordinate and schedule patient visits and study-related procedures.
Collect medical history and support follow-up care and lab procedures.
Maintain adherence to Institutional Review Board (IRB)-approved protocols.
Support the safety and monitoring of research participants.

Communication & Relationship Management:

Build strong, respectful relationships with investigators and office staff.
Maintain effective communication with study teams and cross-functional stakeholders.

Compliance & Documentation:

Follow study protocols, informed consent guidelines, and SOPs.
Comply with all applicable sponsor, company, and regulatory policies and procedures.

Qualifications:

Education: Minimum Associate’s degree or equivalent education and experience.
Experience:
- At least 1 year of experience in a clinical research setting preferred.
- Familiarity with clinical trials and Good Clinical Practice (GCP) principles.
Skills & Knowledge:
- Knowledge of study protocols, procedures, and consent forms.
- Understanding of medical terminology.
- Ability to perform required clinical procedures.
- Detail-oriented with excellent interpersonal skills.
- Ability to work collaboratively with teams, patients, and clients.
Certifications & Licenses: Must meet applicable regulatory requirements.

Note: This position is not eligible for sponsorship.

Additional Information:

Job Tags: #LI-CES #LI-DNP #LI-HCP #ONSITE
Equal Opportunity Employer: IQVIA considers all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or other legally protected characteristics.
Learn more: https://jobs.iqvia.com/eoe

How to Apply:

Visit https://jobs.iqvia.com and search for Job ID R1501959 or click Apply Now.

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Site Research Assistant - Lake Forest, Ca

Job Description

Job Title: Site Research Assistant

Company Overview:

Position Summary:

Key Responsibilities:

Clinical Trial Support:

Communication & Relationship Management:

Compliance & Documentation:

Qualifications:

Additional Information:

How to Apply:

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