Regulatory Affairs Professional, RA Diabetes, CV, Liver and Rare Disease

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Do you have a talent for navigating complex regulatory landscapes and driving strategic initiatives? Are you eager to contribute to the rapid development of a high impact program? 

If you are passionate about regulatory science and committed to bringing innovative medicines to market, then we invite you to apply and join Novo Nordisk as a Regulatory Affairs Professional.

Your new role

As a Regulatory Affairs Professional you will be working within the RA Diabetes, CV, Liver and Rare Disease therapeutic area on several early development projects approaching phase 1 clinical trials. You will belong to one team but also support other teams on similar tasks and be responsible for driving several regulatory tasks with challenging and often overlapping timelines. Therefore, this role entails interactions with various stakeholders throughout the organization.

Your responsibilities may include:

• Contribute with regulatory expertise to global strategies and tactics
• Develop regulatory documentation for submission to Health Authorities globally, e.g. clinical trial applications, briefing packages, paediatric plans, and responses to health authority questions
• Represent Regulatory Affairs in global clinical trial teams and other cross-functional teams
• Collaborate effectively with cross-functional stakeholders such as project managers, medical and non-medical specialists, statisticians, and medical writers

Your new department 

RA Diabetes, CV, Liver and Rare Disease is an area within Regulatory, Quality & Clinical Reporting consisting almost 100 dedicated and highly engaged Global Regulatory Leads, Regulatory Specialists and Professionals, organised in eight teams. Our area is charged with developing and executing on global regulatory strategies. These strategies are designed to advance projects across multiple indications, from the early stages of development through to worldwide submission and approval of initial Marketing Authorisation applications.

We are responsible for driving label development, facilitating interactions with health authorities, and overseeing regulatory submissions. These submissions include initial marketing authorisation applications, paediatric plans, and clinical trial applications. We maintain strong ties with our affiliates and global stakeholders, fostering a close collaboration that is integral to our operations.

Your skills and qualifications

To thrive and succeed in this position you should preferably have:

• A master’s degree or PhD within Life Science, Health Science, or a related field
• Solid and hands-on regulatory and/or drug development experience
• Experience from working on clinical development programs is an advantage 
• Advanced communication skills in both written and spoken English
• Strong IT/digital skills

Personally, you thrive in fast-paced, collaborative environments and actively contribute to the team's success. You should be well-organised, possess robust problem-solving capabilities, and maintain a strategic focus. A positive, can-do attitude is crucial, as is the ability to keep your spirits high and maintain a healthy sense of humour under pressure.

Working 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. The video below features colleagues worldwide speaking about why they’re proud to work at Novo Nordisk and highlights the culture, collaboration and long-term impact. Together, for the long-term! 

What we offer  

At Novo Nordisk, you’ll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage.  

Salary: For this role, the Annual Base Salary ranges from DKK 570,200 to DKK 838,100 (DK), corresponding to the level of the position.

The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.

Incentives and Benefits: The salary package may include short-term as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.  

Learn more about our Reward Philosophy here.  

Contact

For further information, please contact Jenny Kastberg at JYKA@novonordisk.com.

Deadline

17th may

You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Please assist us in maintaining a fair and inclusive selection process by not attaching a photo to your application.

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