Job Title: Site Research Assistant
Location: San Dimas, California (Office-based)
Job ID: R1510626
Employment Type: Part-Time
Work Setup: On-site
Scheduled Hours: 24 hours per week
Additional Locations: San Dimas, California
Overview
IQVIA is seeking a Site Research Assistant to support the conduct of clinical trial activities in compliance with Good Clinical Practice (GCP) and regulatory requirements. This role demands strong organizational skills, logical thinking, and the ability to adapt quickly in a dynamic research environment. The assistant will play a vital role in data management, patient coordination, and study documentation within an on-site research team.
Key Responsibilities
Study Coordination
Assist with screening, recruitment, and enrollment of research participants.
Support informed consent discussions and ensure adherence to IRB-approved protocols.
Coordinate study visits, procedures, and follow-up care per study timelines.
Collect patient histories and perform scheduling of subjects and research procedures.
Monitor participant safety and report any protocol deviations.
Develop and maintain strong working relationships with investigators and site staff to ensure smooth study operations.
Data Management
Enter study data into Electronic Data Capture (EDC) systems accurately.
Resolve data queries promptly and ensure data integrity.
Maintain compliance with sponsor and company Standard Operating Procedures (SOPs) and guidelines.
Ensure all study documentation is accurate, current, and audit-ready.
Collaboration & Communication
Build and maintain strong communication channels with study team members, investigators, and office staff.
Coordinate effectively with laboratory and clinical teams for protocol-related activities.
Participate in team discussions to ensure consistent execution of study goals.
Qualifications
Education & Experience
Minimum: Associate’s Degree or equivalent education and experience.
1+ year of experience in a clinical research environment preferred.
Technical Skills
Solid understanding of clinical trials and Good Clinical Practice (GCP) principles.
Familiarity with protocols, informed consent processes, and study documentation.
Proficient in medical terminology and clinical procedure execution.
Strong attention to detail and accuracy in documentation.
Soft Skills
Excellent organizational, communication, and team collaboration abilities.
Ability to maintain effective relationships with patients, physicians, and internal staff.
Other Requirements
Certifications or licenses as required by company or local regulations.
This position is not eligible for sponsorship.
Compensation
Base Pay Range: $25.00 – $39.00 per hour
Actual pay determined by education, experience, and location.
Additional compensation opportunities may include:
Performance incentives
Health and welfare benefits
Bonus programs
About IQVIA
IQVIA is a global leader in clinical research and healthcare data intelligence, committed to advancing medical innovation and improving patient outcomes. Through our integrated data analytics and technology solutions, we accelerate the development and commercialization of life-saving therapies.
🔗 Learn more: https://jobs.iqvia.com
🌐 Equal Opportunity Employer: IQVIA provides equal employment opportunities regardless of race, color, religion, gender, sexual orientation, identity, national origin, disability, or veteran status.
🔗 https://jobs.iqvia.com/eoe
Application
Apply Now to be part of a team that’s transforming clinical research and advancing healthcare innovation.
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