Clinical Research Associate: Site Monitoring & Compliance
Listed on 2026-10-18
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist -
Healthcare
Clinical Research
IQVIA is a leading global provider of clinical research services. We seek a Clinical Research Associate to perform site monitoring visits, ensure sites conduct the study per protocol, and report data in alignment with GCP and ICH guidelines.
The role requires at least two years of independent on-site CRA monitoring experience, strong communication, and proficiency with EDC, CTMS, eTMF, and standard MS Office tools. Join us to support project teams and drive quality across studies.
This posting is for the Clinical Research Associate:
Site Monitoring & Compliance role at IQVIA, based in San Fernando, CA, United States.
The Clinical Research Associate:
Site Monitoring & Compliance position in the Bio & Pharmacology & Health field is open for applications.
We have an opening for a Clinical Research Associate:
Site Monitoring & Compliance in San Fernando, CA, United States within Bio & Pharmacology & Health.
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