Sr. Non-Clinical Biostatistician
Company: Sanofi
Location: Kissimmee
Posted on: December 1, 2025
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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, Kissimmee , Sr. Non-Clinical Biostatistician, Science, Research & Development , Kissimmee, Florida
