Sundheds-job i Storkøbenhavn
Are you able to cut through complexity and drive regulatory strategies for high-impact projects? Would you like to work together with experts across multiple functions in a global environment? Then join Global Regulatory Affairs in Novo Nordisk and be our new Senior Regulatory Professional for the development project and be part of an exciting environment where engaged people are committed to gain approval of Novo Nordisk’s medicines to bring innovative treatment to patients across the globe. We have a unique combination of scientific insight, patient focus, and the ability to navigate many agendas and stakeholders. That makes RA a truly interesting and dynamic place to work. Apply now for a life-changing career! The position As a Senior Regulatory Professional in our area, you will be part of a fantastic team of 13 people. You will work closely with the Global Regulatory Lead and a team of regulatory professionals and be responsible for driving several clinical regulatory activities within a late-stage development project. You will be a member of cross-functional project and submission teams, and as such, interact with a variety of stakeholders from different departments in Novo Nordisk. Your tasks will include: