• Lead and own all in vitro and in vivo non-clinical toxicology activities (non-GLP & GLP) for multiple programs • Design and communicate customized toxicology strategies for each program • Attend program meetings, collaborate with cross-functional team leads, and guide project team leaders regarding toxicology and safety plans and timelines • Plan, design, and oversee the execution of all outsourced CRO collaborations for toxicology and safety studies • Manage, edit, and finalize collaborators’ (CRO) study reports • Analyze, interpret, present, and communicate all preclinical toxicology and safety study findings • Make key recommendations to project teams for mitigation strategies and next steps • Author high-quality regulatory documents to support filings such as IND, CTA, NDA, and IB