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Clinical Research Coordinator Associate

VIVA • Stanford, CA, US • published 2026-11-06 00:59:38.724703

Description

Hybrid and onsite 4 days/wk during training then 3\-4 per week Clinical Research Coordinator Associate (CRCA) **JOB PURPOSE:** Perform **duties** related to the coordination of clinical studies. Coordinate moderately complex aspects of one or more clinical studies and work under close direction of the principal investigator and/or study coordinator/supervisor CORE **DUTIES:** Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start\-up through closeout. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study specimens and processing. Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms. Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed. Assemble study kits for study visits, monito...

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