Global Study Associate

Global Study Associate

Introduction to role: This role is based in Barcelona, with an on‑site commitment of three days a week. Fluency in English is required.

Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto.

Are you ready to keep pivotal early oncology studies inspection‑ready and moving at pace, so promising science reaches patients sooner? Do you thrive on orchestrating complex, multi‑country clinical work where your coordination, precision and initiative directly influence trial momentum and decision‑making?

Accountabilities

• Trial Master File stewardship: Set up, maintain and close out a complete, compliant TMF; coordinate regular quality checks and proactively address gaps to ensure continual inspection readiness.
• Document production and publishing readiness: Prepare study documents with strict template and version control; ensure packages are complete and ready for publishing in...

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