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Kaiser Permanente
Overview
Collects data for clinical trials and supports the preparation of regulatory documentation for IRB approval. Manages research activities including patient recruitment, specimen collection, and ensuring compliance with federal and local regulations.
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Compensation
Salary not listed
Posted
2 days ago
University of Virginia
The coordinator will manage clinical trial activities, including recruiting and consenting participants, collecting and analyzing study data, and processing laboratory specimens. They are also responsible for maintaining study documentation and submitting protocols to the Institutional Review Board.
$25 - $27 / HOUR
21 days ago
