Senior Director (QSP), Clinical Pharmacology & Pharmacometrics, Research Business Insights/Information Technology

Role: Senior Director for Clinical Pharmacology & Pharmacometrics at Bristol Myers Squibb, leading the development, implementation, and scaling of quantitative workflows, modeling environments, and automation tools to support drug development from preclinical through clinical phases. Responsibilities: oversee CPP technology stack, partner with R&D teams to integrate workflows with scientific and operational capabilities, ensure operational excellence, regulatory readiness, and continuous improvement of modeling systems, and lead a team of scientific technologists and engineers. Requirements: Ph.D. in Pharmacometrics, Clinical Pharmacology, or related field; 12+ years in pharmaceutical R&D with deep expertise in clinical pharmacology, pharmacometrics, PBPK, QSP, and model-informed decision-making; proven experience with regulatory submissions, automation, and AI/ML applications; senior leadership experience with team building and stakeholder engagement. HighValue: focus on model-informed drug development, quantitative workflows, regulatory support, AI-enabled automation, and scalable CPP technology; collaboration with translational labs and data teams. WorkSetup: not specified, but operates within a highly matrixed R&D environment.