Safety Surveillance Principal Specialist (Denmark, Søborg)

Opportunity summary

Employment type: FULLTIME. Jobbeskrivelse Placering Søborg, Denmark Jobkategori Reg Affairs & Safety Pharmacovigilance Ansøg nu Safety Surveillance Post-Marketing Cardiometabolic III Søborg, Denmark Are you driven by patient safety and scientific excellence? Do you want to influence strategic safety decisions for medicines that can improve the lives of millions of patients worldwide? We are looking for a Safety Surveillance Principal Specialist to strengthen our Safety Surveillance Post-Marketing team. If you thrive on solving complex challenges with positive impact on patient safety, and working at the intersection of science, drug development and regulatory strategy — we would love to hear from you. Your new role We are seeking a highly experienced individual to lead high‑impact activities across the incretin portfolio. In this role, you will help set the direction for safety surveillance, drive governance and decision-making and ensure relevant input to our continued development activities and act as a trusted safety leader to key stakeholders. Clear communication, sound judgement, and taking ownership will be essential parts of your workday. As a Safety Surveillance Principal Specialist, you will lead the safety surveillance strategy for Q&A with Health Authorities around the world mainly within diabetes and obesity treatment1 …

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