Senior Clinical Research Site Monitor
Listed on 2026-10-06
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Research/Development
Clinical Research
IQVIA LLC is seeking a Clinical Research Monitor to oversee site monitoring and management, ensuring studies are conducted per protocol and regulatory requirements. You will perform site visits, support data reporting, and work closely with study teams to maintain quality and timelines.
The role requires at least 2 years of on-site monitoring experience, strong communication and organizational skills, and proficiency with MS Office. Visa sponsorship is not available for this position.
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Join us at IQVIA LLC as our next Senior Clinical Research Site Monitor in England, United Kingdom.
We are currently recruiting a Senior Clinical Research Site Monitor for our team in England, United Kingdom.
This is an excellent opportunity to take on the Senior Clinical Research Site Monitor role at IQVIA LLC.
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