Associate Director, Biostatistics

Role: Associate Director of Biostatistics within development teams, contributing to trial design, statistical analysis, and regulatory documentation for clinical studies. Responsibilities include designing innovative trials, defending protocols, authoring key documents, supporting health authority interactions, and managing multiple studies to ensure consistency within a therapeutic area. The role emphasizes collaboration with cross-functional teams, applying advanced statistical methodologies, and maintaining compliance with standards. Leadership duties involve mentoring team members and guiding development strategies. Qualifications: PhD or MS in statistics/biostatistics with 6+ (PhD) or 8+ (MS) years of relevant clinical trial or drug development experience. Proficiency in SAS, R, or Python; strong communication, organizational, and project management skills. Preferred: experience with regulatory interactions and leadership in statistical teams. High-Value: Focus on clinical development, statistical methodology, and regulatory compliance in biopharma, with an emphasis on innovative trial design, external collaboration, and contribution to the broader statistical community. Location: Hybrid or onsite, with some travel expected; roles may be site-essential or hybrid based on the occupancy structure.