Associate Director, Statistics

Role: Lead statistical expert in Medical Affairs & Health Technology Assessment (MA&HTA), providing biostatistical support for drug development, evidence generation, and HTA submissions across therapeutic areas. Responsibilities: design and review scientific protocols, develop innovative statistical methodologies, evaluate data sources including real-world databases, ensure GxP compliance, and support evidence-based decision-making for life-cycle management. Collaborate with cross-functional teams including Medical Affairs, Market Access, Data Sciences, and Regulatory, contributing to research proposals, RWE studies, scientific publications, and HTA submissions. Qualifications: MS (10+ years) or PhD (6+ years) in Statistics/Biostatistics; extensive experience in trial design, real-world data analysis, statistical modeling, and programming; industry experience in regulated biopharma environments, with knowledge of drug development and lifecycle strategies. Preferred skills include expertise in observational study methodologies, confounding control, and bias reduction. High-value: focus on real-world evidence, HTA submissions, cross-disciplinary collaboration, leadership in managing teams, and experience in regulated pharmaceutical development. Work setup and travel details are not specified.