Lisbeth Lyme

Lisbeth Lyme is a seasoned professional with 25 years of experience in Regulatory Affairs, specializing in both CMC and Clinical areas. Currently serving as the Senior Director of Regulatory Affairs at IO Biotech, Lisbeth has held various key positions, including the Regulatory Department Manager at Novo Nordisk and Director of Regulatory Science at IWA Consulting. They have managed teams across multiple high-profile projects, including life cycle management for notable pharmaceutical products. Lisbeth’s academic background includes a degree focused on medicinal product innovation from Copenhagen Business School and a Certificate of Advanced Studies in Pharmaceutical Medicine from the University of Basel.