Sr. Manager, Statistics
Takeda
August 22, 2026
Remote
United States
$137,000 - $215,270 USD yearly
Clinical Research and Development
POSITION DESCRIPTION (Sr. Manager, Statistics)
- Provide statistical support in the design, analysis, and interpretation of clinical trials to enable quantitative decision-making at a compound level for oncology programs.
- Independently represent statistics on global teams in support of drug development.
- Develop and review study synopsis, protocol, statistical analysis plan, clinical study report, and other regulatory submission documents; ensure accurate, statistically valid deliverables.
- Leverage internal and external resources to achieve quality, timely, and cost-effective compound-level and submission deliverables.
- Plan and direct compound-level analysis and reporting activities, including work of other statisticians and programmers.
- Monitor and contribute to industry advances in statistical methods; optimize study designs and statistical analysis methods; implement innovative approaches.
- Up to 100% remote work allowed from anywhere in the U.S.
REQUIREMENTS
- Ph.D. in Mathematics, Biostatistics, Statistics, or related field, plus 1 year of related experience.
- Experience with innovative clinical study designs, complex analytical methods, and inferential statistics; ability to conduct mathematical and statistical simulations.
- Hands-on data analysis using programming languages/software such as SAS, R, Matlab, etc.
- Extensive knowledge of FDA and ICH regulations and industry standards for clinical trials and regulatory submissions.
- Oversight of statistical activities (e.g., SDTM/ADaM standards, TFLs) to ensure timeline and quality.
Benefits (if applicable)
- Medical, dental, vision insurance, 401(k) with company match, short-term/long-term disability, basic life insurance, tuition reimbursement, paid volunteer time off, company holidays, well-being benefits; up to 80 hours sick time/year; up to 120 hours paid vacation accrual for new hires.
Application
- Apply at https://jobs.takeda.com (Job # R0187499).
- Provide statistical support in the design, analysis, and interpretation of clinical trials to enable quantitative decision-making at a compound level for oncology programs.
- Independently represent statistics on global teams in support of drug development.
- Develop and review study synopsis, protocol, statistical analysis plan, clinical study report, and other regulatory submission documents; ensure accurate, statistically valid deliverables.
- Leverage internal and external resources to achieve quality, timely, and cost-effective compound-level and submission deliverables.
- Plan and direct compound-level analysis and reporting activities, including work of other statisticians and programmers.
- Monitor and contribute to industry advances in statistical methods; optimize study designs and statistical analysis methods; implement innovative approaches.
- Up to 100% remote work allowed from anywhere in the U.S.
REQUIREMENTS
- Ph.D. in Mathematics, Biostatistics, Statistics, or related field, plus 1 year of related experience.
- Experience with innovative clinical study designs, complex analytical methods, and inferential statistics; ability to conduct mathematical and statistical simulations.
- Hands-on data analysis using programming languages/software such as SAS, R, Matlab, etc.
- Extensive knowledge of FDA and ICH regulations and industry standards for clinical trials and regulatory submissions.
- Oversight of statistical activities (e.g., SDTM/ADaM standards, TFLs) to ensure timeline and quality.
Benefits (if applicable)
- Medical, dental, vision insurance, 401(k) with company match, short-term/long-term disability, basic life insurance, tuition reimbursement, paid volunteer time off, company holidays, well-being benefits; up to 80 hours sick time/year; up to 120 hours paid vacation accrual for new hires.
Application
- Apply at https://jobs.takeda.com (Job # R0187499).