You will develop and implement safety strategies for a portfolio of projects in various indications with a focus on new modalities, but also including small and large molecules and ADC’s. You will serve as the main interface between Global Program Teams and Nonclinical Safety Global Project Strategy and Science (PSS), ensuring alignment and effective communication. You will analyze toxicology and safety pharmacology data and collaborate with cross-functional teams to ensure effective implementation of safety strategies. You will author nonclinical safety sections of various regulatory documents. You will provide expertise in due diligence reviews and offer recommendations for partnerships or in-licensing opportunities.