Job Description

IQVIA is seeking a Freelance Site Activation Specialist based in Norway, Sweden, or Denmark to oversee clinical trial start-up and site management. The ideal candidate will possess a strong understanding of local regulations and have 2–3+ years of related experience.

Responsibilities include managing site activation, preparing regulatory documentation, and ensuring compliance with ICH-GCP standards. This role is available immediately on a freelance basis, with work flexibility.

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