Senior Regulatory Professional

Novo Nordisk A/S • Søborg, Capital Region of Denmark • Posted June 17, 2026

About the Role

Regulatory Affairs
Søborg, Denmark

Do you want to be part of an exciting environment where engaged people are committed to optimising Novo Nordisk’s medicines across the globe? If yes, join us! We are looking for a Senior Regulatory Professional.

Your new role

As Senior Regulatory Professional, you will take part in developing regulatory strategies and lead execution via interactions with cross‑functional teams. This will entail close collaboration with the Global Regulatory Lead and the rest of the Regulatory Affairs team.

Your main responsibilities will include:

  • Becoming a member of cross‑functional project teams including study groups and submission teams, interacting with a wide range of stakeholders
  • Participating in the development of regulatory documentation for submission to Health Authorities, including briefing packages, clinical trial applications, protocols, reports and regulatory files for mark...