IQVIA seeks an experienced Freelance Site Activation Specialist in the United Kingdom to support clinical trial start-up and site activation tasks. The role focuses on UK submission document collection, site document review, ICF adaptations, and regulatory submission support.
You will work closely with investigative sites and internal teams to ensure submission packages are complete, compliant, and delivered on schedule.
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Remote UK Site Activation Specialist (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.
