AncillaryDocumentCoordinator(Frenchspeaker)

_**Job title:** Ancillary Document Coordinator_ _**Location:** Budapest, Hungary_ _**Job type:** Permanent, full-time_ _**Hybrid working**_ # **About the job** Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? Join our global regulatory affairs team as an **Ancillary Document Coordinator** and you’ll help us request all ancillary document types intended to be submitted for the GRA portfolio, from standard to complex. You’ll be responsible for the operational ancillary document planning request, ability to prioritize workload, and negotiate timelines with key stakeholders. You’ll also partner closely with Vendors to execute the preparation and / or request of the ancillary Documents according to the planning. ## **Main responsibilities:** * Manage end‑to‑end ancillary document requests by applying strong project management skills and expert regulatory knowledge, including country‑specific requirements * Act as a subject‑matter expert, advising cross‑functional stakeholders on ancillary document regulations, guidance, and submission requirements to ensure shared understanding and compliance * Create, maintain, and continuously improve standardized ancillary document templates to support high‑quality, timely submissions aligned with Sanofi and Health Authority standards * Draft, review, and submit CPPs; interact directly with French Health Authorities to request CPPs and GMP certificates as required * Coordinate with external vendors and internal stakeholders to