RA Cagri & CagriSema Diabetes
Søborg, Denmark
Do you want to be part of an exciting environment where engaged people are committed to optimize Novo Nordisk’s medicines across the globe? Would you like to join a team with a unique combination of scientific insight, patient focus, and the ability to navigate many agendas and stakeholders?
If yes, join us as a Regulatory Affairs Specialist.
Regulatory Affairs (RA) is a truly interesting and challenging place to work, so apply today!
Your new role
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 and Amylin portfolio. This will entail close collaboration with the Global Regulatory Lead.
Your main responsibilities will include:
Contributing with regulatory expertise to global strategies and tactics, by analysing regulatory opportunities and risks Leading major submission tracks such as briefing packages for meetings with Health Authorities, clinical trial applications, and global submission strategies, working with affiliates to ensure alignment between local and global regulatory strategies and timely preparation of documentation
You will report to the head of the department and take active part in department related activities, including improvement projects across RA.
Your new department
The Obesity & Cardiometabolic Health (RA OCH) area is responsible for defining and driving regulatory strategies for Novo Nordisk’s Obesity and Diabetes portfolio. We work as an integrated part of the global development and research projects and play a key role in the cross-functional teams. We are responsible for the regulatory strategy and provide regulatory expertise and tactics to the product development plans. We drive label development, health authority interactions and global submission strategies. Our team collaborates closely with affiliates and global stakeholders in the regulatory teams.
Your skills & qualifications
We are looking for a person with a strong regulatory and scientific foundation who can contribute effectively to global regulatory activities. You should be able to work independently within a cross-functional environment and demonstrate sound decision-making based on regulatory principles.
To succeed in this role, you bring:
A Master’s degree or Ph.D. in science, pharmaceutical or health science Minimum 7-8 years of experience in Regulatory Affairs or other relevant area in drug development Practical knowledge in defining and developing global regulatory strategies and good all-around understanding of the regulatory documentation and requirements for pharmaceutical development and licensing Excellent project management skills and ability to cooperate at any organizational level Change-oriented approach and a willingness to experiment Strong communication skills in verbal and written English
On a personal level, you bring a proactive and positive approach, communicate effectively across the organization and work well in dynamic situations. You are comfortable sharing your perspective, approaching challenges with curiosity and flexibility, and taking ownership of your work and continuous development. You stay focused under pressure, adapt to change with ease and contribute constructively to collaborative problem-solving.
Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.
Deadline
15 February 2026. Applications will be evaluated continuously when received and candidates may be called for interview before the deadline.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.