Site Monitoring CRA II — GCP/ICH Expert
Listed on 2026-10-25
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Research/Development
Clinical Research
IQVIA UK Site Management team seeks junior and experienced Clinical Research professionals to perform on-site monitoring visits across multiple sponsors. You will drive subject recruitment plans, train site staff on the protocol, and ensure regulatory compliance throughout the study lifecycle.
The role requires independent monitoring experience, strong GCP/ICH knowledge, and willingness to travel between sites. UK visa sponsorship is not available for this position.
Our organisation is growing, and we are hiring a Site Monitoring CRA II — GCP/ICH Expert in Leeds, England, United Kingdom.
Step into the Site Monitoring CRA II — GCP/ICH Expert role at IQVIA LLC in Leeds, England, United Kingdom and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
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