Sascha Honig

Sascha Honig has extensive experience in regulatory affairs and safety operations, currently serving as Vice President in RA Submissions at Novo Nordisk since September 2003. Key responsibilities include overseeing eCTD submissions for marketing authorization applications and clinical trial applications, driving digital transformation within Global Regulatory Affairs, and ensuring compliance with global event adjudication regulations. Prior roles include Acting Head of RA Submission & Compliance and Senior Director of RA Business Transformation, where Sascha focused on digital transformation initiatives and operational excellence. Earlier positions included leadership roles in safety operations and project management at Novo Nordisk and clinical experience as a registered nurse at Rigshospitalet. Sascha holds a degree in Marketing from Copenhagen Business School and a nursing degree from København Amts Sygeplejeskole.