Senior Director Biostatistics

Role: Senior Biostatistician overseeing statistical activities in oncology clinical development programs. Responsibilities include leading statistical analyses across multiple trials, contributing to study design, authoring statistical sections in protocols and reports, supporting regulatory submissions, and managing CROs. The position involves strategic input on trial design, statistical modeling, data review, and interpretation, with a focus on advancing oncology therapies, particularly in areas like KRAS-mutated cancers. Requirements: PhD in statistics or related field with 13+ years (PhD) or MS with 15+ years of relevant clinical trial experience; expertise in statistical methods for clinical trials, FDA/EMA/ICH regulations, and proficiency in SAS (required) and R (plus). Oncology and regulatory submission experience are preferred. Collaboration involves cross-functional teams including clinical, regulatory, and data management. The role may include contributions to publications and clinical study report writing. Work setup details and travel expectations are not specified.