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Site Research Assistant

1 years
$25.00 - $39.00 per hour
10 Sept. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/ B.Pharma/ M.Pharma/ 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

🏷️ Job Title

Site Research Assistant
Location: Los Angeles, California
Job ID: R1503631
Work Setup: On-site (Office-based)
Job Type: Part-Time (40 hours/week)
Additional locations available

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🧭 Job Profile Summary

Assist in conducting clinical trial activities in compliance with applicable regulations. Key skills include logical thinking, prioritization, adaptability to changing business conditions, and strong interpersonal/team-building abilities.


🔑 Responsibilities

  • Enter data into Electronic Data Capture (EDC) systems and resolve queries.

  • Build and maintain strong working relationships with study team members, investigators, and clinic staff to foster trust and respect.

  • Assist with screening, recruiting, and enrolling research subjects.

  • Schedule patient/research participant visits and coordinate follow-up care and laboratory procedures.

  • Collect patient/research participant medical history.

  • Adhere to IRB-approved protocols and assist in the informed consent process.

  • Support the safety of research subjects during the study.

  • Coordinate protocol-related research procedures, study visits, and follow-ups.

  • Ensure compliance with company, Sponsor policies, Standard Operating Procedures (SOPs), and guidelines.


🎓 Qualifications

  • Minimum of an Associate’s degree or equivalent education and experience.

  • At least 1 year of experience in a clinical research setting preferred.

  • Working knowledge of clinical trials and Good Clinical Practices (GCP).

  • In-depth understanding of study-specific protocols, consent forms, and schedules.

  • Skillful in carrying out required clinical procedures.

  • Familiarity with medical terminology.

  • Detail-oriented with the ability to maintain effective working relationships with coworkers, managers, patients, physicians, and clients.

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

  • Note: This position is not eligible for sponsorship.


💼 Compensation & Benefits

  • Hourly pay range: $25.00 - $39.00 per hour

  • Actual pay may vary based on qualifications, experience, location, and schedule (full/part-time).

  • Incentive plans, bonuses, and other compensation forms may be offered, along with health and welfare benefits.


🌐 About IQVIA

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, accelerating the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.

Learn more: https://jobs.iqvia.com


⚖️ Equal Opportunity Employer Statement

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

More details: https://jobs.iqvia.com/eoe


📩 Ready to apply?

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