Senior Principal Statistician

A company is looking for a Senior Principal Statistician. Key Responsibilities Lead statistical design and analysis for Phase I to IV clinical studies and regulatory filings Collaborate with cross-functional teams to optimize study designs and ensure timely delivery of reports Develop and validate statistical programs, write statistical analysis plans, and prepare for meetings with regulatory agencies Required Qualifications, Training, and Education 2 years of experience Proficiency in SAS and R programming, with knowledge of CDISC models and standards Experience with clinical trial design, complex statistical methods, and regulatory guidelines Knowledge of oncology or hematology therapeutic areas is preferred Experience with Bayesian and adaptive design is a plus