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 and preparation, site document review, ICF adaptations, and regulatory submission support, working with investigative sites and internal study teams to ensure timely, compliant submissions.
The successful candidate will collaborate with Site Activation Managers, Regulatory Affairs,
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Remote UK Site Activation Specialist (Freelance) in Cambridge employer: IQVIA Argentina
IQVIA is an excellent employer that fosters a collaborative and innovative work culture, providing its employees with the opportunity to grow professionally while working on impactful financial reporting across Europe. With a strong emphasis on employee development and proficiency in leading financial systems like PeopleSoft and SAP, team members can expect meaningful career advancement in a supportive environment that values integrity and excellence.
