? (15h Left) Associate Statistical Project Leader
Company: Sanofi
Location: Cambridge
Posted on: June 25, 2025
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Job Description:
Job Title: Associate Statistical Project Leader Location:
Morristown, NJ, Cambridge, MA About the Job Are you ready to shape
the future of medicine? The race is on to speed up drug discovery
and development to find answers for patients and their families.
Your skills could be critical in helping our teams accelerate
Progress. 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. You’ll 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, you’ll 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. We are an innovative global healthcare company
with one purpose: to chase the miracles of science to improve
people’s lives. We’re also a company where you can flourish and
grow your career, with countless opportunities to explore, make
connections with people, and stretch the limits of what you thought
was possible. Ready to get started? 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 validity 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/MS in statistics or related discipline with at
least 3 years of pharmaceutical experience in clinical development,
including experience with Biotech, pharma, Clinical Research
Organizations (CROs), health authorities and 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. - Demonstrated strong
interpersonal and communication skills. - 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 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-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, Pawtucket , ? (15h Left) Associate Statistical Project Leader, Science, Research & Development , Cambridge, Rhode Island
