Clinical Research Associate: Site Monitoring Expert
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, ensure protocol compliance, and manage data and regulatory tasks in line with GCP and ICH guidelines. The role involves site visits, training, and close collaboration with study teams to support project delivery.
Candidates should have a scientific or healthcare degree and at least 2 years of on-site CRA experience in a CRO or sponsor setting, with strong communication and organizational skills.
This role, Clinical Research Associate:
Site Monitoring Expert at IQVIA, could be your next opportunity.
We invite applications for the Clinical Research Associate:
Site Monitoring Expert position located in Denver, CO, United States.
The following position is for a Clinical Research Associate:
Site Monitoring Expert with IQVIA.
Our team is growing, and we are hiring a Clinical Research Associate:
Site Monitoring Expert in Denver, CO, United States.
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