Associate Statistical Project Leader
Company: Sanofi
Location: Cambridge
Posted on: March 13, 2026
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Job Description:
Job Title: Associate Statistical Project Leader Location:
Cambridge, MA, Morristown, NJ About the Job Join the engine of
Sanofis mission where deep immunoscience meets bold, AI-powered
research. In R&D, youll drive breakthroughs that could turn the
impossible into possible for millions. Join our Biostatistics
Immunology & Inflammation (I&I) as Associate Statistical
Project Leader and you will lead several I&I phase 2 or 3
studies under minimum supervision of statistical project leader
and/or team leader. Youll have opportunities to develop innovative
statistical solutions to support critical trial decision-making and
advance treatment across all phases of drug development. Within our
department of Evidence Generation and Decision Science, youll be
supported by a Biostatistics group that fosters people development,
offering compelling career opportunities that value diversity of
thought and abilities, to optimize overall success and have a
meaningful impact on patients lives. About Sanofi: Were an
R&D-driven, AI-powered biopharma company committed to improving
peoples lives and delivering compelling growth. Our deep
understanding of the immune system and innovative pipeline enables
us to invent medicines and vaccines that treat and protect millions
of people around the world. Together, we chase the miracles of
science to improve peoples lives. Main Responsibilities: Provide
high quality input into the design of the clinical study (including
protocol development), the setup and conduct of the study to make
sure data are adequately captured and collected to answer the study
objectives and to support the planned statistical analyses.
Accountable for all statistical deliverables related to the study:
statistical sections in protocol including sample size calculation,
randomization specifications, and statistical methodology, etc.,
Statistical Analysis plan, data surveillance, statistical analysis
results for CSR and its appendices. Effectively utilize external
groups, e.g. CROs or data monitoring committees (DMC). Work with
the programming team to provide definitions, documentation and
review of derived variables, as well as the quality control plan.
Perform and/or coordinate with study programmer the production of
statistical analyses. Review and examine statistical data
distributions/properties. Oversee execution of the statistical
analyses according to the SAP, prepare statistical methods &
provide statistical insight into interpretation and discussion of
results sections for the clinical study report (CSR) and/or
publications to ensure the statistical integrity and scientific
validty of the content according to internal standards and
regulatory guidelines and in compliance with SOPs. Propose, prepare
and perform exploratory data analyses, ad-hoc analyses as relevant
for the study or project objectives. About You PhD in Statistics,
or related quantitative discipline strongly preferred and will be
given preference in candidate selection due to the advanced
statistical methodology required for this role. MS in Statistics or
related discipline required as minimum qualification. A minimum of
3 years of pharmaceutical experience in clinical development, such
as in Biotech, Pharma, Clinical Research Organizations (CROs),
health authorities, or academic clinical research centers. Broad
knowledge and good understanding of advanced statistical concepts
and techniques; being able to do advanced statistical analyses
using SAS or R. Proficient in written and spoken English 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 its 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. Play a critical role
in accelerating Sanofis leadership in the flagship therapeutic area
of Immunology & Inflammation Work closely with leaders and partners
with diverse backgrounds, expertise and styles who are ready to
help you succeed in the organization. Embark on a fast track of
professional growth and development, where you'll gain valuable
skills via projects, connect with industry leaders, and position
yourself for leadership roles in your field 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-SA LI-SA LI-Onsite 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, Revere , Associate Statistical Project Leader, Science, Research & Development , Cambridge, Massachusetts
