Associate Director, Biostatistics and Statistical Programming

This role offers an opportunity to lead critical statistical activities supporting the development of innovative pharmaceutical products across multiple clinical programs. The Associate Director will oversee biostatistical strategy and vendor-delivered statistical programming while ensuring high-quality analysis aligned with regulatory standards and project timelines. Working closely with cross-functional teams including clinical development, data management, and external research partners, you will contribute to study design, protocol development, and the interpretation of complex clinical data. This position plays a key role in shaping statistical approaches across the drug development lifecycle while ensuring data integrity and scientific rigor. The role is ideal for an experienced biostatistics professional who thrives in collaborative environments and enjoys translating data into actionable insights that advance clinical research. Candidates will have the opportunity to influence study outcomes and support regulatory submissions in a fast-paced, innovation-driven setting.