IQVIA is seeking an experienced Freelance Site Activation Specialist in the United Kingdom to support clinical trial start-up and site activation. Focus on UK document collection, site review and regulatory submissions, with ICF adaptations and regulatory support across project timelines.
The role requires home-based UK work, immediate start, approximately 3–6 months, and collaboration with cross-functional teams to ensure compliant submission packages and Green Light readiness.
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Remote UK Site Activation Specialist 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.
