IQVIA LLC 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, site document review, ICF adaptations and regulatory submission support.
You will collaborate with investigative sites and internal study teams to ensure submission packages are complete, compliant, and delivered on project timelines, maintaining adherence to ICH-GCP and UK
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Remote UK Site Activation Specialist - Freelance (3-6m) employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
