IQVIA is seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial start-up and site activation activities. The role focuses on UK submission document collection, site document review, ICF adaptations, and regulatory submission support, working with sites and internal study teams to ensure timely, compliant submissions.
The candidate will manage documentation, timelines, and cross-functional collaboration to ensure Green Light readiness and
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UK Site Activation Specialist - Remote Freelance employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
