Regulatory Integration Lead

Regulatory Integration Lead

This role offers a rare and exciting opportunity to shape how Regulatory, Quality, and Clinical Reporting (RQ&C) teams manage data integrations in the dynamic world of mergers and acquisitions. As the Regulatory Integration Lead, you’ll be at the forefront of connecting innovation, compliance, and technology—driving digital transformation across a global, high-impact organization.

Your new role

As Regulatory Integration Lead, you will drive activities that enable us to manage regulatory activities across a dynamic product portfolio, with a primary focus on securing a smooth and effective integration of core documents into our digital regulatory management platform Veeva RIM in connection with acquisitions.

• Collaborating with cross-functional product teams to develop and implement integration plans, ensuring alignment with business objectives and timelines.
• Leading the migration of regulatory documents into Veeva RIM in connection with acquisitions, ensuring a smooth transition and compliance with regulatory requirements.
• Monitoring and reporting on the progress of integration activities, identifying and mitigating risks as necessary.
• Provide guidance and support to project teams, ensuring adherence to regulatory standards and best practices.
• Improve the standard integration process and drive adoption by product teams and document owners.
• Leveraging digital solutions and AI to secure process scalability, robustness, and compliance.

Your new department

You will have the unique opportunity to be part of RQ&C Operations where you will join the Publishing DK department that plays a key role in ensuring compliant electronic regulatory submissions to Health Authorities. RQ&C Operations is an exciting area involved across the value chain of Novo Nordisk. We are responsible for driving and streamlining the submission and labelling operations to obtain best in class labels as well as effective and compliant regulatory submissions for current and future products, responsive to the worldwide business needs of Novo Nordisk. You will work in a fast-paced environment where it is important to be able to manage deadlines in a complex context of international communication across time zones, cultures, and circumstances. The atmosphere in the team is informal, and good humour is always welcome.

Your skills and qualifications

The ideal candidate has:

• A M.Sc. in a relevant field, such as science, pharmacy, or equivalent.
• Minimum 5 years of experience in the pharmaceutical industry, preferably within Regulatory Affairs.
• Experience working with Veeva RIM or other regulatory IT platforms is required.
• Experience working with process design/improvements and project management is an advantage.
• High proficiency in English

As a person, you are curious to learn, well organised, and a proactive problem solver. You enjoy working in a diverse team and being part of a global project-centric organisation and you are a strong collaborator. You thrive in a dynamic environment and have a can-do attitude as well as a healthy sense of humour. Working with matrix teams, you focus on jointly moving projects, work independently, and bring an innovative mindset seeking novel solutions to the challenges we face.

Working at Novo Nordisk:

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination, and a constant curiosity. For over 100 years, this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect, and a willingness to go beyond what we know delivers extraordinary results.

What We Offer:

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

More Information:

For further information, please contact Associate Director, Robert Navy Lund, on +45 30799943

Deadline

25 November 2025.