The Director of Toxicology is accountable for timely and effective drug safety support for programs in non-clinical and clinical development. The incumbent is expected to support non-clinical development through the design, management and regulatory submissions of all non-clinical safety studies for the company’s drug development programs, as well as provide expertise and guidance in Regulatory Toxicology to project teams and management. This individual will be highly analytical, decisive, goal-oriented, and timeline sensitive while maintaining the highest of scientific and ethical standards. The incumbent will be an active participant on project/program teams, and will work closely with other functional areas such as Discovery Biology, Pharmacology, Medicinal Chemistry, DMPK, CMC and Clinical. The incumbent will manage contracts and budgets and provide study monitoring for outsourced GLP toxicology studies and will provide appropriate content and submission-ready documentation for the toxicology components of regulatory submissions.