Clinical Research Assistant
Los Angeles, Canada · Part Time
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- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 2 hours ago
- Work mode
- In office
- Education
- High school diploma or equivalent
- Eligibility
- Candidates with a high school diploma or equivalent who can work part time onsite in Los Angeles, CA and are interested in supporting clinical research operations may apply.
- Resume
- Required to apply
Where you'll work
Job description
Role overview
The Clinical Research Assistant works alongside Clinical Research Coordinators to help carry out study activities and keep protocol-specific work on track. The position requires careful compliance with ICH, GCP, site rules, and study procedures.
Key duties
- Set up and maintain patient files for each assigned study.
- Prepare for participant visits by making sure source records, assessments, lab kits, and other visit materials are complete and accurate.
- File lab reports, EKG results, and other study communications into the correct patient records.
- Track and replenish study supplies, including lab kits, assessment tools, and materials for participants.
- Enter study data and resolve queries within sponsor timelines and contract deadlines.
- Support coordinators with tasks such as blood pressure checks, urine collection, lab draws, and other assessments.
- Coordinate with participants, caregivers, outside vendors, and laboratories as needed.
- Help with scheduling, copying, faxing, and related administrative work.
- Assist with study monitoring visits.
- Handle day-to-day assignments given by the CRC in support of the study and participants.
- Take on additional duties as assigned, including general office tasks such as restocking exam rooms, ordering supplies, and answering calls.
Education, experience, and skills
- A high school diploma or equivalent is required.
- Strong computer ability and familiarity with office and electronic equipment such as email, computers, fax machines, and copiers are important.
- You should be highly organized and comfortable maintaining records accurately.
- Attention to detail and a strong sense of initiative are needed.
- You must be able to communicate clearly, both verbally and in writing.
- Experience in healthcare, research, or a clinical environment is helpful.
- Basic understanding of clinical research processes and regulations such as GCP, FDA, and IRB is an advantage.
Additional information
This is a part-time onsite role based in Los Angeles, CA.
The job summary and responsibilities indicate a support-focused research operations position with both participant-facing and administrative responsibilities.