Clinical Research Associate: Site Monitoring & Study Delivery
Listed on 2026-10-15
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
IQVIA is seeking an on-site Clinical Research Associate to monitor study sites, ensure data quality, and drive regulatory compliance. You will manage site visits, recruit tracking, training, and documentation across multiple trials while liaising with the study team.
Qualifications include a science/healthcare degree and at least 2 years of CRA experience, with proficiency in EDC, CTMS, eTMF and MS Office. This is a full-time, on-site US-based position with IQVIA.
Consider building your career as a Clinical Research Associate:
Site Monitoring & Study Delivery at IQVIA.
As a Clinical Research Associate:
Site Monitoring & Study Delivery, you will play an important part at IQVIA in Carlsbad, CA, United States.
We invite applications for the Clinical Research Associate:
Site Monitoring & Study Delivery position located in Carlsbad, CA, United States.
The following role is for a Clinical Research Associate:
Site Monitoring & Study Delivery with IQVIA.
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