Senior Director Oncology Biostatistics

Role: Senior Director of Oncology Biostatistics, leading statistical functions for oncology drug development within a global biopharma. Responsibilities: oversee study design, analysis strategies, and regulatory submissions; guide statisticians to ensure high-quality, timely deliverables; manage resources and budgets across multiple oncology programs; contribute to Clinical Development Plans and serve as a key interface with regulatory agencies; drive process improvements, develop SOPs, and represent the company in professional societies. Qualifications: PhD or MS in statistics/biostatistics with 12+ years in clinical trials, drug development, or healthcare; proficiency in SAS, R, or Python; strong communication and organizational skills; extensive experience in global regulatory interactions; minimum 5 years of management experience preferred. High-Value: oncology (specific indications not detailed), clinical trial phases (implied late-stage development), regulatory submissions, GxP compliance, cross-functional collaboration with clinical, regulatory, and statistical teams. Work setup: likely hybrid or onsite depending on location; travel details not specified.