full-time
Manager, Statistical Programmer, Statistical and Quantitative Sciences Japan
Takeda
- Employer
- Takeda
- Location
- Japan
- Working pattern
- on-site
About the role
Lead statistical programming deliverables for clinical studies, integrated analyses, and Japan regulatory submissions, including CDISC-compliant electronic data submissions and agency interactions. Manage study budgets and schedules, collaborate with global teams on standards, improve programming processes and tools, and guide colleagues. Requires a bachelor’s degree or higher in information science, statistics, or a related field, substantial pharmaceutical clinical development experience, and strong statistical programming expertise. Candidates should have advanced SAS skills, knowledge of CDISC and regulatory guidance, and strong English communication and collaboration skills.