Leading the planning, design, execution and interpretation of nonclinical toxicology programs in support of IND, CTA and BLA submissions, including general toxicity and reproductive and developmental toxicology studies, in alignment with global regulatory expectations and program strategy Serving as the primary scientific interface with contract research organizations (CROs), providing strategic oversight during protocol development, study conduct, data interpretation, and report finalization to ensure timely, high-quality, and GLP‑compliant delivery of nonclinical studies Representing the Nonclinical Safety function as a core member of cross‑functional discovery and development program teams, contributing toxicology expertise to inform candidate selection, risk assessment, and overall program advancement Providing critical scientific assessment of toxicology data and communicating clear, actionable risk‑benefit evaluations and recommendations to ...