• lead the biostatistics, data management, and statistical programming functions across all clinical programs • serve as a core member of the clinical development leadership team, contributing to portfolio strategy, asset prioritization, and program governance • provide statistical leadership for oncology trial design, including adaptive designs, Bayesian approaches, biomarker-driven studies, and complex endpoints (e.g., OS, PFS, ORR, MRD) • guide development strategies from first-in-human through registrational and post-marketing studies • act as the statistical authority in interactions with global regulatory agencies (FDA, EMA, PMDA, etc.) • oversee the statistical and data components of INDs, NDAs, BLAs, MAAs, and responses to regulatory questions • ensure timely, high-quality delivery of statistical analyses, datasets, TFLs, and clinical study reports • oversee CRO and vendor strategy for data management and programming • establish scalable processes, standards, and infrastructure to support a growing oncology pipeline • drive innovation in data review, analytics, and visualization to enable real-time decision-making • build, mentor, and retain a high-performing, multidisciplinary team across biostatistics, data management, and statistical programming • partner closely with Clinical Development, Clinical Operations, Regulatory Affairs, Translational Medicine, Medical Affairs, and Commercial teams.