Angel City VA Recruitment

Clinical Research Assistant

Angel City VA Recruitment

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.

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