Onsite Clinical Research Associate – Flexible Monitoring & Study Support

IQVIA LLP is seeking an experienced Clinical Research Associate to perform on-site monitoring visits in the UK, ensure protocol adherence, and manage site communications. You will support recruitment planning, training, and documentation to maintain regulatory compliance and data integrity across interventional studies.

The role requires at least 2 years of on-site monitoring experience, a degree in a scientific discipline or health care, and full UK right to work, with visa sponsorship not

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