Safety Surveillance Early Development

Søborg, Denmark

Are you passionate about ensuring patient safety in drug development? Do you thrive in a dynamic and collaborative environment where scientific excellence and meaningful impact are at the forefront? If so, we invite you to become our new Safety Surveillance Principal Specialist at Novo Nordisk. Read on and apply today!

Your new role

The Safety Surveillance Early Development team is part of Global Patient Safety, and we handle all First Human Dose (FHD) studies across all indications at Novo Nordisk. As a Safety Surveillance Principal Specialist, you'll be the safety lead for several products in our early pipeline, working at the crossroad of non-clinical and clinical development.

In this role you’ll: