Clinical Research Associate: Field Monitoring Pro
Listed on 2026-10-18
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
IQVIA is seeking a Clinical Research Associate to monitor study sites and manage data in line with the protocol, applicable regulations, and sponsor requirements. You will perform site visits, oversee recruitment plans, and ensure regulatory filing and data integrity.
The role requires at least 2 years of independent on-site monitoring experience and proficiency with EDC/CTMS/eTMF. Strong English communication and collaboration with study teams are essential.
Step into the Clinical Research Associate:
Field Monitoring Pro role at IQVIA in Santa Cruz, CA, United States and grow with us.
Learn more about the Clinical Research Associate:
Field Monitoring Pro role in the description above.
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