IQVIA is seeking a Freelance CRA to support clinical trial activities in the UK. Location: United Kingdom with travel across the UK for site visits; 0.5-0.7 FTE, start asap, duration about 1 year.
You will participate in monitoring Phase I-IV trials and coordinate with CTM/Lead CRA to ensure study requirements are met. Responsibilities include site evaluation, initiation visits, ongoing monitoring, data validation, and preparation of monitoring reports.
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