Locations: 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
Company: IQVIA
The Site Research Assistant supports clinical trial activities under established protocols and regulatory guidelines. This individual plays a vital role in patient interaction, data collection, study coordination, and overall support of clinical research operations. The role is ideal for candidates who demonstrate strong attention to detail, adaptability, and team collaboration.
Assist in screening, recruiting, and enrolling research subjects.
Perform participant scheduling and coordinate follow-up visits and lab procedures.
Support protocol-related research procedures and ensure adherence to IRB-approved protocols.
Assist in the informed consent process.
Perform Electronic Data Capture (EDC) entry and resolve queries.
Collect and record patient history and source documentation accurately.
Maintain study schedules, consent forms, and protocol-specific documentation.
Build and maintain effective communication with investigators, clinical office staff, and study team members.
Support participant safety and compliance throughout the clinical trial lifecycle.
Develop strong, respectful working relationships within the clinical and research environment.
Adhere to Good Clinical Practice (GCP) standards, regulatory requirements, and company/Sponsor SOPs.
Schedule and track subject visits and study procedures as per protocol guidelines.
Education: Minimum of an associate’s degree or equivalent combination of education and experience.
Experience:
At least 1 year of experience in a clinical research setting preferred.
Familiarity with clinical trial operations and procedures.
Skills & Knowledge:
Understanding of clinical trials, protocols, and Good Clinical Practices (GCP).
Working knowledge of medical terminology and clinical documentation.
Detail-oriented with strong organizational and interpersonal skills.
Ability to build effective relationships with patients, study teams, physicians, and clients.
Certifications & Licensing:
Must hold any applicable certifications or licenses required by regulatory authorities or the company.
Note: This position is not eligible for sponsorship.
Hourly Pay Range: $25.00 – $39.00
(Final pay will be determined based on experience, education, skills, and location.)
May include additional incentives, bonuses, and a comprehensive range of health, wellness, and retirement benefits.
IQVIA is a global leader in clinical research, healthcare intelligence, and data analytics. We connect data, technology, and insights to drive innovation in the life sciences industry, supporting better patient outcomes and public health solutions.
Learn more: https://jobs.iqvia.com
IQVIA is committed to equal employment opportunities. All qualified applicants will receive consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or other legally protected status.
EEO Policy: https://jobs.iqvia.com/eoe
Search for Job ID: R1501959 at https://jobs.iqvia.com or click Apply Now to begin your application.
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