Sr Dir, In- Vivo & Non Clinical Pharmacology -Cambridge Crossing MA

Senior Director For In-Vivo & Non-Clinical Pharmacology Bristol Myers Squibb is seeking a strategic and scientifically grounded leader to serve as the Senior Director for In-Vivo & Non-Clinical Pharmacology. This leader will partner deeply with Research leadership and the Pharmacology, DMPK, Toxicology, and Translational Science units to deliver the applications, workflow capabilities, AI, and supporting data flows that enable non-clinical decisions across in-vivo biology, DMPK, ADME, non-clinical safety, toxicology, and bioanalytical science. The role is focused on the digital and analytical capability layer that helps Research generate, interpret, and act on non-clinical evidence, rather than owning the underlying scientific operations themselves. In close partnership with BMS's R&D Data organization and peer BI&T leaders, this role will help build an integrated, multi-year environment in which non-clinical evidence flows cleanly into translational, clinical pharmacology, regulatory, and Development decision-making. Reporting to the Vice President, Research Business Insights & Technology, this leader will operate as part of a unified BI&T leadership team and act as a trusted partner to Research leadership, translating scientific needs into scalable, integrated technology solutions. Mission & Impact Enable higher-confidence candidate progression decisions through integrated non-clinical applications, AI, and workflow support Modernize PK/PD, DMPK/ADME, toxicology, and bioanalytical decision environments with predictive and AI-enabled capabilities Improve how non-clinical evidence is captured, connected, and reused to support downstream translational, clinical pharmacology, regulatory, and Development decisions Advance predictive safety, translational modeling support, histopathology image AI, and agent-enabled study workflows where they create clear scientific value Reduce fragmentation across non-clinical workflows and improve decision speed, traceability, and reuse of evidence Key Responsibilities Partner with Pharmacology, DMPK, Toxicology, and Translational Science leaders to shape and deliver the technology roadmap supporting non-clinical decisions Lead deployment of GenAI, agentic, and predictive AI/ML capabilities for non-clinical workflows, including predictive safety, in silico DMPK, histopathology image AI, and study design support Ensure non-clinical data is captured with high fidelity in source systems and flows cleanly to downstream curation by the R&D Data organization Partner with scientific, quality, and operational stakeholders to ensure applications appropriately support animal welfare data, IACUC-related processes, and study-governance workflows Enable non-clinical safety signal detection and risk characterization through modern analytics, integrated data flows, and decision-support tools Partner with Development teams so that clinical findings flow back into non-clinical model validation and refinement Ensure operational excellence and reliability of non-clinical applications, modeling environments, and analytics Lead and develop a team of scientific technologists, AI/ML engineers, product leaders, and application specialists