Clinical Research Associate II - Onsite Monitoring

IQVIA UK is seeking an experienced Clinical Research Associate to join the cFSP team in Manchester, performing on-site monitoring visits and ensuring compliance with GCP/ICH guidelines. You will coordinate with sites, manage recruitment plans, and support study documentation and TMF/ISF maintenance.

The role requires at least 2 years of on-site monitoring experience in interventional studies, a scientific or healthcare degree, and valid UK work eligibility.