Safety Surveillance Early DevelopmentSøborg, 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 roleThe 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:Lead the analytical and medical evaluation of emerging aggregate safety data from pre‑clinical and clinical studies to establish the product’s early safety profileSolve unique and complex safety challenges that impacts patient surveillance ...