HEVA Business Partner Multiple Myeloma
Company: Sanofi EU
Location: Cambridge
Posted on: May 10, 2025
Job Description:
Job Title: Director, HEVA Business Partner - Multiple
MyelomaLocation: Cambridge, MA, Morristown, NJAbout the JobSanofi
Specialty Care has pioneered the development and delivery of
transformative therapies for patients affected by debilitating
diseases for over 30 years. We accomplish our goals through
world-class research, collaboration with the global patient
community, and with the compassion and commitment of our employees.
With a focus on rare diseases, multiple sclerosis and
onco-immunology, we are dedicated to making a positive impact on
the lives of the patients and families we serve. Sanofi Specialty
Care's portfolio of transformative therapies, which are marketed in
countries around the world, represent ground-breaking and
life-saving advances in medicine. Sanofi Specialty Care employees
benefit from the reach and resources of one of the world's largest
pharmaceutical companies with a shared commitment to improving the
lives of patients.Sanofi's Oncology franchise has a diverse and
fast-growing portfolio. This includes late-stage launching
candidates in multiple myeloma and lung cancer as well as several
promising compounds in the pipeline targeting hematologic
malignancies and solid tumors alike. - -Sarclisa is approved for
relapsed refractory multiple myeloma (RRMM) and is currently being
explored in newly diagnosed multiple myeloma patients. - HEVA's
mission is to conduct, communicate, and translate evidence to
demonstrate the value of Sanofi's products and support optimal
access and treatment outcomes for patients. - The oncology HEVA
team is responsible for designing and fulfilling evidence
generation plans that meet the strategic goals of oncology
portfolio.The HEOR/HEVA business partner in this position will
support Sarclisa upcoming global launches and pipeline indications
in collaboration with the cross functional teams.We are an
innovative global healthcare company, committed to transforming the
lives of people with immune challenges, rare diseases and blood
disorders, cancers, and neurological disorders. From R&D to
sales, our talented teams work together, revolutionizing treatment,
continually improving products, understanding unmet needs, and
connecting communities. We chase the miracles of science every
single day, pursuing progress to make a real impact on millions of
patients around the world.Main Responsibilities:
- This role will be responsible for development of Health
Economic and Outcomes Research (HEOR) strategy and execution of
relevant tactics to support the value proposition of Sarclisa for
multiple myeloma. The incumbent will interface with Market Access,
Clinical, Medical Affairs, and Commercial teams including Global
and US. The role is accountable for the planning, design,
implementation, and completion of innovative evidence-based
research programs that are consistent with product strategies. The
research programs will provide appropriate evidence and/or tools to
be used for internal decision making and for external audiences at
product launch and over product life cycle. -
- This role will be responsible for the design and execution of
Health Economic and Outcomes Research (HEOR) research in the forms
of economic modelling, database analysis, observational research,
systematic literature review, evidence synthesis, value dossier
development and other types of HEOR research.
- This role will also work on HEOR evidence generation priorities
and plan for the assigned oncology indications in life cycle or
under development and incorporate them into broader Sanofi planning
documents such as the integrated evidence generation plan
(IEGP).
- This role will operate as part of a multi-functional global
Brand team and development team that is responsible for designing
clinical research programs to meet the evidentiary standards of
regulators, health technology assessment (HTA) organizations,
reimbursement authorities, third-party payers and other
organizations that review evidence relevant to Sanofi
medicines.
- This role will serve as a subject matter expert to provide
input in various commercial, medical, market access teams, and
strategy development
- This role is expected to demonstrate effective communication,
organizational and interpersonal skills to be able to work
effectively as part of a multidisciplinary team. - The incumbent is
expected to work independently, but in concert with the direction
provided by their management, in accordance with defined functional
policies and precedents, budgetary guidelines, company values,
ethics and applicable law.Key Stakeholders:Internal:
- Market Access & Pricing, Global, US and Ex-US affiliates
- Cross functional Brand team
- Medical Affairs - GBUs, affiliates, HEVA RW Evidence and
Analytics, Clinical Outcomes Generation
- Commercial team
- R&D - Global project teams and Clinical Affairs, Clinical
Outcomes Assessment (COA) and Health Value Translation (HVT)
- Public Affairs, Communications
- Regulatory Affairs, Compliance and LegalExternal:
- Payers/Reimbursement Authorities
- Key Opinion Leaders (KOLs)
- Health Technology Assessment (HTAs) and other review bodiesKey
Performance Indicators
- Timely design and execution of the HEVA plan
- Demonstrated contributions to product success
- Development and execution of strategies that address data gaps
and customer needs
- Expertise recognized within the function
- Develops and maintains peer relationships to establish HEVA as
an expert in HEOR.
- Anticipates communication needs to cross-functional audiences
and pre-empts issues with timely and effective action
- Established track record of scientific and/or methods
publications in peer-reviewed journals -
- Compliance with all relevant internal SOPs and external laws
and regulations.About You -
- Advanced degree (PhD, MD, MS, MPH, or PharmD) in a scientific
discipline
- Minimum of 5-7 years of combined experience in health
economics, outcomes research, or a related field
- Demonstrated experience in applying various HEOR methods to
specific research projects and have supported global launches.
- Compliance with all relevant internal SOPs and external laws
and regulations.
- Proficiency in principles of evidence-based medicine and
clinical research methodology, economic modeling, and COAs.
- Understands, creates, and applies relevant methods (e.g.,
observational data, post hoc analysis of clinical trials,
meta-analysis, indirect comparison, etc..) to demonstrate product
value potential
- Provided recommendations to clinical development programs aimed
at ensuring differentiation for payer value demonstration
- Has experience in translating Target Value Propositions and
access strategies into evidence hypotheses, requirements and
generation plans addressing payer/provider/health system unmet
needs
- Publication in peer-reviewed journals
- Knowledge of global HTA processes and guidelines, experience
with HTA submissions preferred
- Knowledge of US payers and guidelines, experience with US
submissions preferred
- Strong ability to partner with colleagues from other (i.e.
non-HEOR) functional areas
- Demonstrated understanding disease physiopathology, drug
mechanism of action, clinical development principles, epidemiology,
biostatistics, statistical programming COA development, systemic
literature reviews, and network meta-analyses -Skills &
Competencies:
- English fluent, both written and oral
- Strong communication skills, both verbal and written, including
presentation skills. Significant experience making presentations to
senior management is strongly desired
- Understanding of the legal and regulatory environment of the
pharmaceutical industry, demonstrated integrity on work-related
compliance considerations and solid ethics
- Entrepreneurial and team spirit and ability to develop creative
solutions to complex problemsWhy 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
Keywords: Sanofi EU, East Hartford , HEVA Business Partner Multiple Myeloma, Other , Cambridge, Connecticut
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