HEOR Biostatistician
Company: Sanofi
Location: Morristown
Posted on: June 25, 2025
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Job Description:
Job Title: HEOR Biostatistician Location: Cambridge, MA
Morristown, NJ Level: Sr. Manager/Associate Director equivalent
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 Global
Health economics and Outcome Research Team as a HEOR
Biostatistician and you’ll Serve as Project Lead within Global HEVA
and across multiple therapeutic areas to conduct post-hoc analysis
of clinical trials in support of market access and reimbursement
evidence needs. In this role, you will be held scientifically
accountable at global and local levels for design and timely
execution of post-hoc statistical analyses for HTA submissions and
pricing/reimbursement negotiations. You will also support countries
for local HTA submissions and provide statistical expertise within
HEVA that aligns with several stakeholders including Market Access
and Pricing, Medical Affairs, Clinical Outcome Assessment teams,
Biostatistics, etc. 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: - Lead,
design, conduct and QC post-hoc statistical analyses required for
HTA submissions and pricing/reimbursement negotiations - Global:
efficacy in target populations; health-economic modeling
(cost-effectiveness); indirect treatment comparisons; post-hoc
evidence to support development of Payer Value Story and Objection
Handler including analyses to support identification of high burden
subgroups with high likelihood of reimbursement - Country: support
country specific post-hoc requirements for health-economy modeling,
and efficacy in target population and subgroups; work closely with
country market access leads in coordination with Global teams; part
of HTA Rapid Response team and responsible for ensuring timely
completion of any requests from HTA bodies - Present and explain
statistical analyses to team members, internal forum, internal
managers and/or external authors and experts - Publication
activities: Provide consultation, input and guidance to
cross-functional groups charged with development and submission of
manuscripts, posters, slide presentations and abstracts; work with
Publication Leads and team members to respond in a timely manner to
journal editor and reviewer comments - Support clinical teams in
the analyses of clinical outcome assessments (COAs), in particular
patient-reported outcomes (PROs), and Health Economic endpoints for
phase 2 to 4 studies, by contributing and/or reviewing protocols,
statistical analysis plans, clinical study reports, and submission
modules - Psychometric assessment of COAs: Review psychometric
analysis plans and reports, and serve as key statistical contact
for the vendor in charge of the analyses About You Basic
Qualifications & Experience - MSc or PhD in Statistics,
Biostatistics or related quantitative sciences - Minimum 6 years of
experience as a statistician supporting clinical trials, medical
affairs, or clinical development, including conducting statistical
analyses from phase 3 or phase 4 studies, in an industry setting
(ie. pharma, biotech, CRO) Knowledge and Skills - Thorough and
up-to-date knowledge of statistical methods, especially those
related to human clinical studies - Thorough and up-to-date working
knowledge of SAS with hands-on programming experience. Knowledge of
S-PLUS or R is a plus - Working knowledge of SDTM and ADaM data
structure and CDISC standards - Working knowledge of regulatory
guidelines for drug development, NDA submissions, and statistical
practices (ie. CTD guidance, ICH guidelines) - Working knowledge of
PROs; experience in psychometric evaluation is a plus - Knowledge
of HTA technical guidelines (ie. NICE DSU, IQWiG General Methods)
is a plus - Experience publishing results, including writing of
abstracts and manuscripts - Ability to manage projects, to quickly
accommodate changing priorities and to meet tight deadlines while
maintaining high quality standards - Demonstrated leadership,
project management, and interpersonal and negotiation skills, with
excellent verbal and written communication skills - Collaborative
approach; ability to thrive in a fast-paced team environment and to
work independently on projects - Ability to explain strategies,
approaches, methods, analyses, and findings to non-statisticians;
ability to help others interpret results and place in context -
Ability to negotiate and advocate with strong methodological
arguments with the partners to improve quality of the deliverables
and interpretation - Understanding of other functional areas as
well as transversal groups and ability to maintain productive
inter-function working relationships - Experience working with
external service providers - Competencies in written & 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, Hamilton , HEOR Biostatistician, Science, Research & Development , Morristown, New Jersey
