Regulatory Affairs Specialist

Opportunity summary

Do you want to be part of an exciting environment where engaged people are committed to optimize Novo Nordisk’s medicines across the globe? If yes, join us! We are looking for a Regulatory Specialist! Our people have a unique combination of scientific insight, patient focus, and the ability to navigate many agendas and stakeholders. That makes Regulatory Affairs a truly interesting and challenging place to work. The position As Regulatory Affairs Specialist, you will be responsible for developing regulatory strategies and lead their execution via interaction with cross-functional teams. You will lead, drive and coordinate several regulatory activities related to the Novo Nordisk GLP-1 portfolio. This will entail close collaboration with the Global Regulatory Lead. Your responsibilities will include: Contributing regulatory expertise to global development strategies by identifying opportunities, assessing risks, and providing strategic recommendations Leading key regulatory submission activities, including briefing packages for interactions with Health Authorities, clinical trial applications, and global regulatory submission initiatives ensuring high-quality and1 …

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