IQVIA is seeking a Freelance Site Activation Specialist based in the United Kingdom to drive clinical trial start-ups and site activation. The role focuses on UK submission document collection, site document review, ICF adaptations, and regulatory submission support.
You will collaborate with Site Activation Managers, Regulatory Affairs, and cross-functional teams to ensure compliant, complete submission packages delivered on time.
Remote Freelance UK Site Activation Specialist in Oxford 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.
