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Site Research Assistant - San Dimas, Ca

1+ years
$25.00 – $39.00 per hour
10 July 16, 2025
Job Description
Job Type: Remote 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 (Part-time)

Location: San Dimas, California
Job Type: Part-time (24 hours/week)
Compensation: $25.00 – $39.00 per hour
Work Mode: On-site


Job Summary

IQVIA is hiring a Site Research Assistant to join its on-site clinical team in San Dimas, CA. This part-time opportunity (24 hours/week) is ideal for candidates with a background in clinical research or healthcare support. You will play a pivotal role in coordinating patient participation, supporting clinical trial procedures, managing EDC entry, and maintaining GCP compliance. This role requires strong interpersonal skills, adaptability, and attention to detail.

Join one of the world’s leading clinical research organizations and contribute to cutting-edge pharmaceutical and healthcare innovations.


Key Responsibilities

  • Perform EDC data entry and manage query resolution

  • Build effective communication with study teams, investigators, and clinic staff

  • Support participant screening, recruitment, and enrollment

  • Manage patient scheduling, history collection, and follow-up coordination

  • Assist with informed consent process and ensure IRB compliance

  • Conduct protocol-related procedures and study visits

  • Adhere to all SOPs, regulatory guidelines, and sponsor requirements

  • Maintain accurate documentation and ensure participant safety throughout


Required Skills & Qualifications

  • High school diploma or equivalent

  • Minimum 1 year of experience in a clinical research setting preferred

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

  • Familiarity with medical terminology and study protocols

  • Strong attention to detail, organizational, and time management skills

  • Ability to build positive relationships with team members, patients, and investigators

  • Certifications and licenses as required by regulatory bodies


Perks & Benefits

  • Competitive hourly compensation: $25.00 – $39.00

  • Opportunity to work on cutting-edge clinical trials

  • Gain valuable hands-on experience in clinical research coordination

  • Contribute to meaningful healthcare advancements

  • Join a globally recognized leader in life sciences and pharmaceutical research


Company Description

IQVIA is a global leader in clinical research, healthcare analytics, and real-world evidence. Serving top pharmaceutical and life sciences organizations, IQVIA delivers data-driven solutions that accelerate clinical trials and enhance patient outcomes.


Work Mode

On-site – San Dimas, California


Call to Action

Looking to grow your career in clinical research? Apply now to join IQVIA as a Site Research Assistant and help shape the future of pharmaceutical innovation from the ground up.