Collaborate with Regulatory Affairs and/or R&D on creation and review of regulatory (EMA and FDA) and clinical content and documentation, related to new drugs, clinical trials, as well as medical treatments (e.g. parts of clinical dossier module 2.5, scientific advice requests, brochures' clinical parts) - with focus on epidemiology, therapeutic area or indication background, national and international guidelines and patient journey/medical need, based on study reports, medical-scientific publications and other literature and key external experts' insights * For your daily work you will collaborate closely cross-functionally with R&D, Regulatory Affairs, Global Safety, Global Marketing, Global Market Access, Global Sales etc.
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