Manager, Statistical Programmer, Statistical and Quantitative Sciences Japan

About the role

Lead statistical programming deliverables for clinical studies and Japan regulatory submissions, including CDISC-compliant data, budgets, schedules, and submission strategies. Collaborate with global teams and stakeholders to standardize programming, improve processes and tools, support agency interactions, and guide colleagues. A bachelor’s degree or higher in information science, statistics, or a related field is required, along with substantial pharmaceutical clinical development and statistical programming experience. Candidates should have advanced SAS skills, knowledge of CDISC and regulatory guidance for statistical programming and electronic submissions, and strong English communication and collaboration skills.