Sr. Manager, Statistics

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionPursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:JOB LOCATION: Cambridge, MAPOSITION: Sr. Manager, StatisticsPOSITION DESCRIPTION: Takeda Development Center Americas, Inc. is seeking a Sr. Manager, Statistics with the following duties: provide statistical support in the design, analysis, and interpretation of clinical trials to enable quantitative decision-making at a compound level for Takeda oncology programs; independently represent statistics function on global teams in support of drug development; develop and review the study synopsis, protocol, statistical analysis plan, clinical study report, and other regulatory submission documents, ensuring accurate and 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 to optimize study designs and statistical analysis methods, and implement innovative approaches at a compound level. Up to 100% remote work allowed from anywhere in the U.S.The estimated salary range reflects an anticipated range for this position. The actual base salary offered will be in accordance w/ state or local min wage requirements for the job location.US based employees may be eligible for short-term &/or long-term incentives. US based employees may be eligible to participate in medical, dental, vision insurance, 401(k) plan & company match, short-term & long-term disability coverage, basic life insurance, tuition reimbursement program, paid volunteer time off, company holidays, & well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, & new hires are eligible to accrue up to 120 hours of paid vacation.REQUIREMENTS: Ph.D. in Mathematics, Biostatistics, Statistics, or related field, plus 1 year of related experience. Prior experience must include: familiarize with innovative clinical study designs, complex analytical methods, and inferential statistics and be able to conduct mathematical and statistical simulations based on those advanced methodologies to support clinical trials; apply advanced knowledge and leverage hands-on experience on data analyses utilizing mathematical and statistical programming software and languages (such as SAS, R, Matlab, etc.) to facilitate drug development processes in pharmaceutical industry; demonstrate extensive knowledge of FDA and ICH regulations and industry standards applicable to the design, conduct and analysis of clinical trials, and regulatory submissions; provide oversight of statistical activities (such as SDTM/ADaM standards, TFLs, etc.) to ensure timeline and quality of analysis data and statistical outputs.Full time. $137,000 - $215,270 per year.Qualified applicants can apply at . Please reference job #R0187499. EOEAny individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeReference: R0187499