Sanofi US Services Inc. Posted August 25, 2026

HEVA Dupixent Business Partner Respiratory Diseases

Cambridge, United States Full time
Market Access Respiratory
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Sanofi US Services Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job title:   HEVA Dupixent Business Partner Respiratory Diseases

Location: Cambridge, MA or Morristown, NJ

About the Job

Sanofi is an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. We apply our deep understanding of the immune system to invent medicines and vaccines that treat and protect millions of people around the world, with an innovative pipeline that could benefit millions more. Our team is guided by one purpose: we chase the miracles of science to improve people's lives; this inspires us to drive progress and deliver positive impact for our people and the communities we serve, by addressing the most urgent healthcare, environmental, and societal challenges of our time.

Dupixent (dupilumab) represents one of the most significant advances in the treatment of Type 2 inflammatory diseases in a generation. As a first-in-class biologic targeting the IL-4/IL-13 pathway, Dupixent has transformed the standard of care for patients living with moderate-to-severe asthma and, most recently, Chronic Obstructive Pulmonary Disease (COPD), becoming the first biologic approved for COPD with a Type 2 inflammatory phenotype.

Sanofi is committed to maximizing the full potential of Dupixent across the respiratory space, building a robust and differentiated evidence base that demonstrates its transformative value to patients, payers, and health systems. Through a focused and rapidly expanding body of clinical and real-world evidence, Sanofi aims to address critical gaps in care and deliver meaningful, potentially life-changing treatment options for the millions of patients living with Type 2 inflammatory respiratory conditions who continue to face significant unmet need.

This role is primarily focused on Dupixent in COPD and Asthma. Depending on business need, the incumbent may also be called upon to support evidence generation activities for other assets within the respiratory or broader Sanofi portfolio.

HEVA Vision, Mission, and Values

We are one bold HEOR team leveraging innovative HEOR to transform patient care and access. As HEOR experts, we lead the generation and dissemination of robust, business-relevant evidence to demonstrate value and drive access to medicines. The HEVA organization is driven by five core values that define how we work and deliver impact. We operate as One Team, partnering without boundaries while pursuing a Bold Purpose through ambitious, measurable goals. Grounded in Scientific Excellence with Relevance and deep technical expertise, we embrace Innovation in Action to transform how we research and deliver Impact for People, creating meaningful outcomes for patients, the healthcare ecosystem, and our colleagues who make it all possible.

This role is accountable for leading US HEOR strategy and execution for Dupixent in respiratory disease, with a primary focus on COPD and Asthma, serving as the primary US HEVA point of contact for the portfolio and partnering cross-functionally to drive the generation, translation, and dissemination of high-quality, decision-relevant evidence to support access in the United States. The role sits at the heart of one of Sanofi's most strategically significant and commercially important portfolios, requiring a combination of deep scientific expertise in respiratory disease and Type 2 inflammation, strategic thinking, and a sophisticated understanding of the US payer and market access landscape.

You will work in the Dupixent Respiratory team of the Health Economics and Value Assessment (HEVA) department. The HEVA department gathers a wealth of expertise including experts in Health Economic and Outcomes Research (HEOR), Indirect Treatment Comparison & Network Meta-Analysis (ITC/NMA), Modelling, Health Technology Assessment (HTA), Evidence Synthesis, Epidemiology, Biostatistics, and generation of Real World Evidence (RWE). Within HEVA Dupixent Respiratory, you will join a team responsible for HEVA projects across multiple indications at various stages of development and lifecycle management.

Join the team transforming care for people with immune challenges, rare diseases, cancers, and Specialty Care neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.

About Sanofi

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s 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 people’s lives.

Main Responsibilities

This role operates independently with minimal supervision, working in concert with management direction in accordance with defined functional policies, budgetary guidelines, company values, ethics, and applicable law. The incumbent mentors junior team members on a case-by-case basis and is expected to develop and maintain peer relationships to establish HEVA as a recognized expert in HEOR.

Strategic Business Impact

Develop and implement US payer-specific HEVA strategy in close collaboration with cross-functional team members to support the launch and lifecycle management of Dupixent in COPD and Asthma

Drive measurable business impact through execution of HEVA tactics that directly support commercial objectives and market access goals compliantly and efficiently

Execute comprehensive US HEVA tactics for the Dupixent Respiratory portfolio, contributing to strategic planning and ensuring alignment with broader portfolio objectives

Partner with commercial teams to translate HEVA insights into actionable business strategies that effectively position Dupixent within the competitive US respiratory market

Partner with access and medical team members to generate and disseminate actionable, high-impact evidence that addresses US payer evidence requirements and value demonstration in a competitive market

Develop business-relevant US research agendas through cross-functional input and alignment, ensuring evidence priorities are reflected in broader Sanofi planning documents, including the Integrated Evidence Generation Plan (IEGP)

Set HEOR evidence generation priorities independently for assigned Dupixent Respiratory indications and translate Target Value Propositions and US market access strategies into evidence hypotheses, requirements, and generation plans that address the unmet needs of payers, providers, and health systems

Support evidence generation activities for other assets within the respiratory or broader Sanofi portfolio as directed by business need

Internal Partnerships and Senior Management Engagement

Build and maintain strong relationships with cross-functional teams, including commercial, medical affairs, clinical development, and market access, to ensure pricing and access decisions are aligned with the demonstrable value of Dupixent in COPD and Asthma

Align closely with the Global HEVA team to ensure US insights inform global strategies and coordinate evidence generation, modeling, and evidence synthesis activities

Communicate complex health economics concepts and strategic recommendations to cross-functional stakeholders with clarity and impact, including presentations to senior leadership

Influence key business decisions through data-driven insights and strategic HEVA recommendations

Ensure clinical development plans for Dupixent Respiratory indications are designed to deliver true differentiation aligned to Sanofi's best-in-class or first-in-class ambition, with particular attention to US payer value demonstration

Contribute to US launch readiness planning for Dupixent Respiratory indications, serving as the HEVA subject matter expert across internal governance forums and brand team meetings

Health Economics Research and Evidence Generation

Lead the design and execution of Health Economic and Outcomes Research (HEOR) activities for Dupixent in COPD and Asthma, spanning multiple indications at various stages of development and lifecycle management

Oversee the design, execution, and publication of high-quality HEOR studies, including economic modeling, database analysis, observational research, Clinical Outcomes Assessment (COA) development and validation, systematic literature reviews, evidence synthesis, and AMCP dossier development

Apply proficiency in economic modeling and COAs to generate evidence that is compelling to US payers, HTA bodies, and other decision-makers in the respiratory space

Understand, create, and apply relevant HEOR methods, including observational data analysis, post hoc analysis of clinical trials, meta-analysis, and indirect treatment comparisons, to demonstrate the value potential of Dupixent and other pipeline assets

Execute all HEVA tactics at the highest level of quality to compliantly further HEOR evidence dissemination, application, and proactive and/or promotional use with US stakeholders (HCEI, PIE)

Apply data-driven decision-making frameworks to prioritize evidence gaps and guide research investment decisions for the Dupixent Respiratory portfolio, ensuring alignment between identified data gaps and strategic evidence generation priorities

Contribute to the development of comprehensive real-world evidence strategies that support product lifecycle management across the Dupixent Respiratory portfolio

Stakeholder Engagement and External Partnerships

Represent Sanofi at major scientific conferences and industry forums, leading abstract development and presentation delivery for the Dupixent Respiratory portfolio

Develop collaborative research relationships with US payers and other key decision-makers to identify strategies that improve the impact of HEOR and build advocates for Sanofi's data in the respiratory space

Collaborate with external research partners and key opinion leaders to advance HEVA strategy and tactical plans for Dupixent in COPD and Asthma

Work with the team lead to engage with external evidence bodies (ICER, PDAB, IRA) and apply knowledge of their requirements to shape evidence generation and value demonstration strategies for the Dupixent Respiratory portfolio

Build and sustain productive working relationships with patient advocacy organizations in the respiratory disease space

Manage HEVA research investments and vendor relationships for assigned Dupixent Respiratory indications, ensuring delivery of evidence generation priorities within budget constraints

Leadership & Team Contribution

Operate independently with minimal supervision, exercising sound scientific and strategic judgment in the design and prioritization of HEOR activities

Mentor junior HEVA team members on a case-by-case basis, sharing expertise in respiratory HEOR methods, US payer dynamics, and evidence generation best practices

Develop and maintain peer relationships across the HEVA organization and with cross-functional partners to establish HEVA as a recognized center of excellence in Dupixent Respiratory HEOR

Anticipate communication needs across cross-functional audiences and pre-empt issues with timely and effective action

Contribute to the continuous improvement of HEVA processes, tools, and capabilities within the Dupixent Respiratory franchise

Regulatory & Compliance Knowledge

Apply knowledge of global and US-specific HTA processes and guidelines; experience with HTA submissions strongly preferred

Ensure all HEOR activities comply with relevant internal SOPs and external laws and regulations

Demonstrate a thorough understanding of the legal and regulatory environment of the pharmaceutical industry, with demonstrated integrity on compliance considerations and solid ethics

Stay current with evolving US payer policies, formulary management practices, and outcomes-based contracting frameworks relevant to respiratory biologics and the COPD and Asthma treatment landscape

Digital & AI Proficiency

Apply working proficiency with HEOR-relevant digital tools and data platforms to enhance the efficiency and quality of evidence generation

Leverage digital and AI-enabled solutions to accelerate systematic literature reviews, evidence synthesis, and economic modeling workflows

Understand the application of real-world data analytics and advanced data platforms to respiratory outcomes research

Maintain foundational knowledge of AI and digital tools relevant to health economics, including familiarity with data analytics platforms; demonstrate willingness to develop proficiency with new AI-enabled solutions to support HEOR research and evidence generation

Stay current with emerging digital methodologies relevant to HEOR and champion their adoption within the Dupixent Respiratory HEVA team

About You

Advanced degree (PhD, MD, MS, MPH, or PharmD) in a scientific discipline required

5+ years of experience in health economics, outcomes research, or a related field

US product launch experience with a strong understanding of US payer evidence requirements and value demonstration in a competitive market

Understanding of US healthcare system and payer dynamics, with ability to translate evidence into strategic insights

Demonstrated experience applying a broad range of HEOR methods to specific research projects, including economic modeling, observational research, evidence synthesis, and COA development

Proficiency in the principles of evidence-based medicine, clinical research methodology, health economic modeling, and patient-reported outcomes

Experience translating Target Value Propositions and market access strategies into evidence hypotheses, requirements, and generation plans that address payer, provider, and health system unmet needs

Experience supporting market access and reimbursement through HEVA evidence (e.g., value tools, evidence summaries, AMCP dossier contributions)

Working knowledge of US evidence dissemination (HCEI/PIE, reactive/proactive, CFL)

Established track record of scientific and/or methods publications in peer-reviewed journals

Knowledge of global HTA processes and guidelines; experience with HTA submissions preferred

Strong ability to partner effectively with colleagues from non-HEOR functional areas, including commercial, medical affairs, clinical development, and market access

Compliance with all relevant internal SOPs and external laws and regulations

Demonstrated understanding of respiratory disease physiopathology, including the mechanisms and clinical manifestations of COPD and Asthma, as well as the role of Type 2 inflammation and the IL-4/IL-13 pathway in driving disease

Knowledge of biologic and targeted therapy mechanisms of action, with specific familiarity with Dupixent's mode of action and its application across respiratory indications

Proficiency in health economic modeling, clinical development principles, epidemiology, biostatistics, COA development, systematic literature reviews, and network meta-analyses

Working proficiency with HEOR-relevant digital tools and data platforms; ability to apply digital solutions to enhance research efficiency and evidence quality

Familiarity with US real-world data sources (e.g., claims databases, electronic health records) and their application to respiratory outcomes research

Experienced in statistical analysis methods relevant to HEOR, including ability to critically evaluate and apply quantitative evidence to support value demonstration and payer engagement

Foundational knowledge of AI and digital tools relevant to health economics, including familiarity with data analytics platforms and digital research tools

Strong communication skills, both verbal and written, including the ability to present complex scientific and strategic content to senior management and cross-functional audiences

Entrepreneurial spirit, team orientation, and the ability to develop creative solutions to complex scientific and business problems

Demonstrated ability to work independently and manage multiple priorities in a fast-paced, matrixed environment

Understanding of the legal and regulatory environment of the pharmaceutical industry; demonstrated integrity on compliance considerations and solid ethics

Preferred Qualifications

Prior experience with Dupixent or other respiratory biologics strongly preferred, including familiarity with the clinical evidence base and value story for Dupixent in COPD and Asthma

Deep knowledge of the COPD and Asthma competitive landscape, including familiarity with approved and emerging biologic and non-biologic treatment options and their payer positioning in the US market

Expertise in Type 2 inflammation biology and its relevance to patient identification, phenotyping, and value demonstration in respiratory disease

Experience supporting US payer advisory boards, formulary submissions, or outcomes-based contracting negotiations in the respiratory or biologics space

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 US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.

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Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.

North America Applicants Only

The salary range for this position is:

$178,500.00 - $257,833.33

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.

Job details

Seniority
Not listed
Function
Market Access
Therapeutic area
Respiratory
Location
Cambridge, United States
Employment type
Full time

How this role compares

Computed from every other active Market Access role in our database, not just this employer's listings.

We currently track 232 comparable Market Access roles across 56 biopharma companies.

232Comparable roles tracked
217Currently active
56Companies hiring similar roles
43Countries represented

Salary context

59 of 232 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $178,500/yr – $257,833/yr
Peer group range $75,510 – $290,000 (median $205,000)

Where these roles are based

Top locations among the 232 comparable roles

United States94
India15
Germany12
China11
Japan8
United Kingdom7

+ 37 more countries

Seniority mix

181 of 232 peers have a known seniority level

Manager73
Director48
Associate Director39
Senior Director8
Senior6
Intern/Fellow/Postdoc3
Executive/VP2
Associate2

Therapeutic area mix

47 of 232 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology17
Rare Disease8
Neuroscience7
Immunology7
Dermatology & Aesthetics4
Ophthalmology3
Cardiovascular / CVRM1

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How we calculate "similar"

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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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