Safety Surveillance Specialist

Your impact begins here As a Safety Surveillance Specialist in the Safety Surveillance Development Cardiovascular Disease (CVD) team, you will help establish and shape the safety profile of new assets moving through clinical development. You will lead the analytical and medical evaluation of emerging aggregate safety data, turning complex findings into clear insights that guide strategic project decisions.

Your work will influence patient surveillance and benefit-risk evaluations across our cardiovascular disease portfolio — helping improve patient lives worldwide. What you’ll bring We are looking for a colleague with a collaborative mindset who thrives on tackling complex safety challenges and turning data into meaningful insights. To succeed in this role, you likely have:

• - A master’s degree within Medicine or Natural Sciences (e.g. MD, DVM, MSc Pharm or equivalent), possibly complemented by a PhD or research experience.
• - Experience within drug development, clinical safety, pharmacovigilance, or other relevant scientific disciplines.
• - A solid understanding of drug development processes, global regulatory requirements, GxP standards, and medical concepts.
• - A proven ability to identify challenges, shape strategies, and translate them into clear, actionable steps1 …