A reputable player in its field, with worldwide HQ in the Lausanne area. Active in the pharmaceutical field and investing significantly in R&D.
Mid-sized, Swiss company with an international presence. Open and pleasant office space, well situated.
Responsible for the strategy for document preparation and writing of documents linked to the company's products : clinical study reports, investigator brochures, briefing books, paediatric investigations, informed consent forms etc.
A cross functional role, interacting with Regulatory Affairs, Medical team, Clinical Scientists and others, it is seen as a subject matter expert in the implementation of best practices in medical writing.