Clinical Research Associate: Site Monitoring & Trial Delivery
Listed on 2026-10-18
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Research/Development
Research Assistant/Associate, Clinical Research -
Healthcare
Clinical Research
IQVIA is seeking an on-site Clinical Research Associate in Berkeley to monitor studies and ensure data integrity and regulatory compliance. You will partner with sites to drive recruitment, manage protocol training, and maintain essential study documents.
The role requires 2+ years as CRA in CRO/sponsor settings, strong knowledge of GCP/ICH, and proficiency with EDC, CTMS, and eTMF systems;
English communication must be excellent.
Join us at IQVIA as our next Clinical Research Associate:
Site Monitoring & Trial Delivery in Berkeley, CA, United States.
As a Clinical Research Associate:
Site Monitoring & Trial Delivery, you will play an important part at IQVIA in Berkeley, CA, United States.
We invite applications for the Clinical Research Associate:
Site Monitoring & Trial Delivery position located in Berkeley, CA, United States.
The following opening is for a Clinical Research Associate:
Site Monitoring & Trial Delivery with IQVIA.
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