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Angel City VA Recruitment

Clinical Research Assistant

Angel City VA Recruitment

Los Angeles, Canada · Tempo parcial

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Experiência
Qualquer
Salário
Vagas
1
Publicado
há 1 semana
Modo de trabalho
No escritório
Educação
Diploma do ensino médio ou equivalente
Elegibilidade
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.
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Onde você trabalhará

Descrição da vaga

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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