Sr. Non-Clinical Biostatistician
Company: Sanofi
Location: Waltham
Posted on: January 12, 2026
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Job Description:
Job Title: Sr. Non-Clinical Biostatistician Location:
Swiftwater, PA About the Job We deliver 4.3 billion healthcare
solutions to people every year, thanks to the flawless planning and
meticulous eye for detail of our Manufacturing & Supply teams. With
your talent and ambition, we can do even more to protect people
from infectious diseases and bring hope to patients and their
families. The Biostatistics Manager of the TED (Translational and
Early Development) team supports Vaccine R&D under the
supervision of the head of Preclinical or Non-Clinical Team and/or
the TED Global head who are all part of the Global Biostatistical
Sciences (GBS) team. As a core objective, his/her responsibilities
include but not limited to provide statistical support in R&D
for pre-clinical work, bioassay and biomarker research and/or CMC,
biological assay, and biomarker research. He/She will work in close
collaboration with the scientists and/or projects managers and
under the supervision of the senior managers of the TED Team.
He/She will assume responsibility for methodological and
statistical aspects of pre-clinical and/or non-clinical studies,
with general direction from Research Project Leader or technicians.
He/she will provide critical input on the design and analysis so
that accurate assessments are made for decision-making, while
ensuring compliance with regulatory expectations. Main
responsibilites Acts as the lead statistician and provides support,
with minimal supervision from manager or TED Global Head, to the
preclinical research team or non-clinical team on statistical
requests and on all relevant statistical matters. His/her
responsibility includes but not limited to: Develop the digital
mindset and data science of the clients under his/her
responsibility (communications, training, etc.). Support the
digital evolution of the site within its scope of activity. Perform
technology watch on data science topics and be the referent for the
platform. Provides statistical input in the design of experiments
with regards to available information and assumptions of in vivo or
in vitro preclinical studies and/or research, clinical and
analytical (CMC) bioassay development. Contribute to the setup of
the study to make sure data are adequately captured and collected
to address the study objectives. Provide statistical support of
experimental design, statistical methodology, statistical
programming, and data analyses. Provide statistical analyses
(planning, prioritization, application forms, analysis reports),
write statistical memos/reports, communicate, and explain to
scientists the statistical conclusions. Accountable for all
statistical operations, including but not limited to: Sample size
calculation and design of experiment, if applicable, Suitability
and compliance of randomization plan, if applicable, Quality,
compliance, and delivery of statistical methodology & statistical
reports. Accountable for the statistical scientific content:
Selects statistical methodology to support the objectives of the
studies, Drives risk assessment for study conclusions if
applicable, Statistical interpretation of results driving study
conclusion, Proposes, prepares, and performs exploratory data
analyses, ad-hoc analyses when applicable. Links with other
internal and external stakeholders (such as R&D compliance,
Functional Planner, Project Manager, CROs, etc.) Under supervision
of the senior manager of the TED team or Research lead,
participates in project activities such as assist in preclinical
development plan, decision-making meetings, integrated analyses and
dossier preparation, submission (IND and CTD) and follow-up
(publication). Acts as representative in internal initiatives
within TED and GBS. Presents internally and externally topics
related to statistical activity. Management activity:
Cross-functional management: Collaborates with more junior
statisticians or contingent workers for the preparation and
production of statistical report & analyses/programming.
Accountable for management of the activities that are outsourced to
external partners (CROs). Education/Experience Education Master's
degree in Statistics with 4 years industry experience OR PhD in
Statistics/Biostatistics with internship in life science Experience
Experience in Life Sciences industries is a must. Technical
expertise in statistics, data science, statistical modelling, etc.
Soft Skills Good communication skills. Ability to work in a
multi-cultural environment. Ability to work in a team (team spirit,
ease of communication). Eager to learn and open-minded. Good time
management. Autonomous. Statistical Tools R, JMP, Other softwares
(e.g. SAS or Phython) is a plus. Language Effective English in
terms of verbal and written communication skills. Why choose us?
Bring the miracles of science to life alongside a supportive,
future-focused team. Discover endless opportunities to grow your
talent and drive your career, whether it’s through a promotion or
lateral move, at home or internationally. Enjoy a thoughtful,
well-crafted rewards package that recognizes your contribution and
amplifies your impact. Take good care of yourself and your family,
with a wide range of health and wellbeing benefits including
high-quality healthcare, prevention and wellness programs and at
least 14 weeks’ gender-neutral parental leave. Sanofi Inc. and its
U.S. affiliates are Equal Opportunity and Affirmative Action
employers committed to a culturally diverse workforce. All
qualified applicants will receive consideration for employment
without regard to race; color; creed; religion; national origin;
age; ancestry; nationality; marital, domestic partnership or civil
union status; sex, gender, gender identity or expression;
affectional or sexual orientation; disability; veteran or military
status or liability for military status; domestic violence victim
status; atypical cellular or blood trait; genetic information
(including the refusal to submit to genetic testing) or any other
characteristic protected by law. GD-SP ? LI-SP vhd? All
compensation will be determined commensurate with demonstrated
experience. Employees may be eligible to participate in Company
employee benefit programs, and additional benefits information can
be found here.
Keywords: Sanofi, Hartford , Sr. Non-Clinical Biostatistician, Science, Research & Development , Waltham, Connecticut