Associate Director, Drug Development Excellence

Role: Associate Director, Drug Development Excellence, focusing on advancing DD strategy and ensuring high-quality execution of cross-functional initiatives within Bristol Myers Squibb. Responsibilities include conducting detailed analysis of end-to-end drug development processes, identifying inefficiencies, and implementing process improvements through re-engineering and digital tools. The role involves developing performance metrics, monitoring KPIs, and supporting digital enablement toward an AI-enabled operating model. Collaboration spans multiple DD domains such as Clinical Development, Trial Operations, Biostatistics, Regulatory, and Safety, with a focus on driving operational excellence and change management. Qualifications: BA/BS required; 5-7 years in operational excellence, process improvement, or strategy roles within pharma, preferably with Drug Development experience. Knowledge of process re-engineering methodologies (Lean, Six Sigma), project management tools, data analytics, and emerging digital technologies including AI. Strong interpersonal, communication, and leadership skills are essential to influence stakeholders and foster continuous improvement. High-value specifics: Focus on process optimization within drug development, digital transformation, and operational excellence initiatives to support clinical and regulatory stages.