Regulatory Medical Writing Program Lead

EU Regulatory Science Lead who is strategic, collaborative and adaptable to join our Global Regulatory Affairs team, based in our Brussels, Belgium offices. About The Role You will drive the EU regulatory strategy and activities for assigned products across development, approval and lifecycle activities. You will be the main regulatory contact for EU health...

A major Belgian financial institution is consolidating three initiatives into one strategic enterprise data transformation program: a Self-Service Data Platform, legacy BI decommissioning and reporting tooling simplification. As Lead Program Manager, you will connect executive governance with delivery across Enterprise Data Platforms, Data Products,...

IQVIA, Brussels-based, seeks a Principal Medical Writer to lead full CSR writing for Phase 1, develop protocols, and prepare regulatory modules 2.7.1/2.7.2. The role emphasizes producing inspection-ready deliverables with strict regulatory and internal guidelines, and requires precise writing and strong English communication.You will manage document shells,...

Mission Overview:The Lead Program Manager consultancy mission is offered by Keystone Solutions, with the consultant working on-site at the client. As a Keystone Solutions consultant, you will represent our values and expertise while delivering strategic transformation in a dynamic client environment.Responsibilities:Define, govern, coordinate, and deliver...

Make your mark for patients We are looking for a DT Lead Medical Affairs who is strategic, collaborative, and results-driven to join us in our Digital Technology Patient Evidence team, based in our HQ office in Brussels, Belgium. About The Role In this global role, you will lead the digital technology strategy and delivery for Medical Affairs systems...

If you're looking for a meaningful job with a dynamic company that uses cutting-edge technology combined with world-class expertise and unbridled enthusiasm, then look no further. At Sobi, we transform the lives of people with rare diseases through our passion for making medicine more accessible and finding new ways to improve people's lives.As a Medical...

Thermo Fisher Scientific is seeking a Senior Medical Writer to lead and deliver high‑quality publications, abstracts, and posters for peri‑ and post‑approval programs. This role emphasizes scientific accuracy, regulatory alignment, and clear communication in English, within a highly collaborative CRO environment.The ideal candidate has extensive...

Join our Brussels team and help solve complex regulatory challenges At ToxMinds, we help leading chemical, biocide, cosmetic and pharmaceutical companies solve their most challenging product safety and regulatory questions. Our reputation is built on scientific excellence, pragmatic regulatory advice, and innovative approaches that combine deep toxicological...

Sobi in Belgium seeks a Medical Advisor in Nephrology & Hematology to drive strategic medical activities and coordinate with global initiatives. You will deliver high-quality medical communications and engage with key external stakeholders.Reporting to the Medical Lead Belux, you will define local medical plans, support cross-functional teams, and help shape...