Director of Biostatistics, Oncology (BOSTON)
Company: Takeda Pharmaceutical
Location: Boston
Posted on: March 25, 2026
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Job Description:
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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 Description Objectives: Takeda is
a global, values-based, R&D-driven, top 15 biopharmaceutical
leader committed to discover and deliver life-transforming
treatments, guided by our commitment to patients, our people and
the planet. Our Data and Quantitative Sciences group (DQS) is made
up of more than 500 quantitative scientists who harness the insight
of data and digital to speed the development of highly innovative
treatments to patients. These scientists (from quantitative
clinical pharmacology, statistics, programming, outcomes research
and epidemiology, patient safety & pharmacovigilance) bring their
expertise to our global program teams and reimagine our
disciplines. They work with novel data streams, including
real-world data and digital tools, and apply advanced analytics
including artificial intelligence and automation. As part of DQS,
the Statistics and Quantitative Sciences (SQS) at Takeda is looking
to add individuals to our team that are team oriented,
collaborative, strong understanding of the statistics function,
exceptional leaders and innovators. SQS aspires to bring safe and
effective medications to the patients with our quantitative skills.
We design efficient trials, contribute to clinical development
strategies, perform high quality statistical analyses, and pursue
operational excellence. About the role: This Senior Manager,
Statistics is responsible for providing statistical support in
clinical development related to diseases and assets within the
Neuroscience Therapeutic Area. This role involves independently
managing projects, providing innovative solutions to problems,
leading data strategy development. This role contributes to
Takeda’s mission. Delivery and Business Accountabilities: - Lead
and be accountable for study/program level delivery - Effectively
drive and influence project teams towards seamless delivery while
enabling and making decisions - Conduct advanced statistical
analyses and perform trial simulations to provide innovative
solutions and to optimize clinical trial designs. - Implement a
quantitative decision making framework to support data-driven
decisions in clinical development - Participate in preparation of
regulatory submissions and responses to regulatory agencies. -
Contribute to asset level strategies to identify and mitigate
delivery risks. - A Senior Manager, Statistics, through her/his
daily work, should have impact on: - Global project sub-teams
(e.g., Evidence Generation) - Broadly DQS functions - Parts R&D
functions Core Skill and Qualification Elements: - Advanced
knowledge of drug development, clinical study designs, trial
simulations, analysis methodology and data interpretation. -
Advanced knowledge of pharmaceutical industry, overall drug
development process and expertise in the cross-functional
interfaces with the statistics function. - Advanced knowledge of
FDA and ICH regulations and industry standards applicable to the
design, analysis of clinical trials and regulatory submissions. -
Strong statistical programming skills (SAS and R) - Excellent oral
and written communications skills. - Specialized statistical
expertise in multiple therapeutic areas or clinical trial
development phases (Experience in Neuroscience preferred). - Strong
project management skills. - Strong collaborative skills and
ability to work with a cross-functional team to achieve project
objectives. Technical/Functional Expertise: A Senior Manager,
Statistics needs to demonstrate: - The capability to gain broader
technical expertise outside of primary area - The ability to
communicate effectively with cross functional teams and explain
statistical and quantitative concepts to non-experts - The drive
for learning techniques and methods and also for continuous
improvement through various avenues of the organization Leadership:
A Senior Manager, Statistics may have to: - Lead projects directly
or indirectly related to Global Program Teams (GPTs) or other
functions - Work independently and prioritize projects -
Effectively drive and influence project teams towards objectives
while enabling and making decisions - Contribute to asset level
strategies - Have internal and external presence on topics of
interest Educations: Applicants for this position should have
degree in statistics/biostatistics or in other equivalent
quantitative sciences along with the following specific
credentials: - PhD with approximately 3 years of experience. - MS
with approximately 6 years of experience. Behavioral Competencies:
An ideal candidate for this position should: - Be able to make
decisions - Initiate and foster collaborative relationships Takeda
Compensation and Benefits Summary We understand compensation is an
important factor as you consider the next step in your career. We
are committed to equitable pay for all employees, and we strive to
be more transparent with our pay practices. For Location: Boston,
MA U.S. Base Salary Range: $137,000.00 - $215,270.00 The estimated
salary range reflects an anticipated range for this position. The
actual base salary offered may depend on a variety of factors,
including the qualifications of the individual applicant for the
position, years of relevant experience, specific and unique skills,
level of education attained, certifications or other professional
licenses held, and the location in which the applicant lives and/or
from which they will be performing the job. The actual base salary
offered will be in accordance with state or local minimum wage
requirements for the job location. U.S. based employees may be
eligible for short-term and/ or long-term incentives. U.S. based
employees may be eligible to participate in medical, dental, vision
insurance, a 401(k) plan and company match, short-term and
long-term disability coverage, basic life insurance, a tuition
reimbursement program, paid volunteer time off, company holidays,
and well-being benefits, among others. U.S. based employees are
also eligible to receive, per calendar year, up to 80 hours of sick
time, and new hires are eligible to accrue up to 120 hours of paid
vacation. EEO Statement Takeda is proud in its commitment to
creating a diverse workforce and providing equal employment
opportunities to all employees and applicants for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, gender expression, parental status, national
origin, age, disability, citizenship status, genetic information or
characteristics, marital status, status as a Vietnam era veteran,
special disabled veteran, or other protected veteran in accordance
with applicable federal, state and local laws, and any other
characteristic protected by law. Locations Boston, MA Worker Type
Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes
It is unlawful in Massachusetts to require or administer a lie
detector test as a condition of employment or continued employment.
An employer who violates this law shall be subject to criminal
penalties and civil liability.
Keywords: Takeda Pharmaceutical, Warwick , Director of Biostatistics, Oncology (BOSTON), Science, Research & Development , Boston, Rhode Island