🏷️ 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
🔗 Apply Now | Save Job | Share: Email | LinkedIn | Facebook
🧭 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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