IQVIA Inc 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.
You will work with investigative sites and internal study teams to ensure submission packages are complete, compliant, and delivered on time, maintaining study trackers and collaborating
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Remote UK Site Activation Specialist (Freelance) employer: IQVIA, Inc.
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous learning opportunities and the chance to work with cutting-edge technology in the heart of the healthcare industry. Join us in a role that not only challenges you but also allows you to make a meaningful impact on global health outcomes.
