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Sanofi

Global pharma company; vaccines and R&D

E4A Dupixent Business Partner Respiratory Diseases

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-time$178.5k - $257.8kIn-person

About the Job

Requirements

  • An advanced degree (PhD, MD, MS, MPH, or PharmD) in a scientific discipline is required.
  • At least five years of experience in health economics, outcomes research, or a related field is required.
  • US product launch experience and a strong understanding of US payer evidence requirements and value demonstration in a competitive market are required.
  • Understanding of the US healthcare system and payer dynamics, with the ability to translate evidence into strategic insights, is required.
  • Demonstrated experience applying a broad range of HEOR methods to research projects, including economic modeling, observational research, evidence synthesis, and COA development, is required.
  • Proficiency in evidence-based medicine, clinical research methodology, health economic modeling, and patient-reported outcomes is required.
  • Experience translating Target Value Propositions and market access strategies into evidence hypotheses, requirements, and generation plans addressing payer, provider, and health system unmet needs is required.
  • Experience supporting market access and reimbursement through HEVA evidence, such as value tools, evidence summaries, and AMCP dossier contributions, is required.
  • Working knowledge of US evidence dissemination, including HCEI/PIE, reactive/proactive, and CFL, is required.
  • An established track record of scientific and/or methods publications in peer-reviewed journals is required.
  • Strong ability to partner with colleagues in commercial, medical affairs, clinical development, and market access is required.
  • Compliance with relevant internal SOPs and external laws and regulations is required.
  • Understanding of respiratory disease physiopathology, including COPD and Asthma mechanisms and clinical manifestations, and the role of Type 2 inflammation and the IL-4/IL-13 pathway, is required.
  • Knowledge of biologic and targeted therapy mechanisms of action, including familiarity with Dupixent's mode of action and application across respiratory indications, is required.
  • Proficiency in health economic modeling, clinical development principles, epidemiology, biostatistics, COA development, systematic literature reviews, and network meta-analyses is required.
  • Working proficiency with HEOR-relevant digital tools and data platforms, and the ability to apply digital solutions to improve research efficiency and evidence quality, is required.
  • Familiarity with US real-world data sources, including claims databases and electronic health records, and their application to respiratory outcomes research, is required.
  • Experience with statistical analysis methods relevant to HEOR, including the ability to critically evaluate and apply quantitative evidence to support value demonstration and payer engagement, is required.
  • Foundational knowledge of AI and digital tools relevant to health economics, including data analytics platforms and digital research tools, is required.
  • Strong verbal and written communication skills, including the ability to present complex scientific and strategic content to senior management and cross-functional audiences, are required.
  • Ability to develop creative solutions to complex scientific and business problems and work independently while managing multiple priorities in a fast-paced, matrixed environment is required.
  • Understanding of the legal and regulatory environment of the pharmaceutical industry, with integrity in compliance considerations and sound ethics, is required.

Responsibilities

  • Develop and implement US payer-specific E4A strategy with cross-functional team members to support the launch and lifecycle management of Dupixent in COPD and Asthma.
  • Execute E4A tactics that support commercial objectives and market access goals compliantly and efficiently, and contribute to strategic planning aligned with portfolio objectives.
  • Partner with commercial teams to translate E4A insights into business strategies positioning Dupixent in the US respiratory market.
  • Partner with access and medical team members to generate and disseminate evidence addressing US payer evidence requirements and value demonstration.
  • Develop business-relevant US research agendas through cross-functional input and alignment, reflecting evidence priorities in Sanofi planning documents, including the Integrated Evidence Generation Plan.
  • Set HEOR evidence-generation priorities for assigned Dupixent Respiratory indications and translate Target Value Propositions and US market access strategies into evidence hypotheses, requirements, and generation plans.
  • Support evidence-generation activities for other assets in the respiratory or broader Sanofi portfolio as business needs direct.
  • Build relationships with commercial, medical affairs, clinical development, and market access teams to align pricing and access decisions with Dupixent's demonstrated value in COPD and Asthma.
  • Align with the Global E4A team so US insights inform global strategies and coordinate evidence generation, modeling, and evidence synthesis.
  • Present complex health economics concepts and strategic recommendations to cross-functional stakeholders and senior leadership.
  • Influence business decisions through data-driven insights and strategic E4A recommendations.
  • Ensure clinical development plans for Dupixent Respiratory indications deliver differentiation aligned with Sanofi's best-in-class or first-in-class ambition, particularly for US payer value demonstration.
  • Contribute to US launch readiness planning as the E4A subject matter expert in internal governance forums and brand team meetings.
  • Lead the design and execution of HEOR activities for Dupixent in COPD and Asthma across indications and lifecycle stages.
  • Oversee design, execution, and publication of HEOR studies, including economic modeling, database analysis, observational research, COA development and validation, systematic literature reviews, evidence synthesis, and AMCP dossier development.
  • Apply economic modeling and COAs to generate evidence relevant to US payers, HTA bodies, and other respiratory decision-makers.
  • Apply HEOR methods, including observational data analysis, post hoc clinical-trial analysis, meta-analysis, and indirect treatment comparisons, to demonstrate the value potential of Dupixent and pipeline assets.
  • Execute HEVA tactics to support compliant HEOR evidence dissemination, application, and proactive or promotional use with US stakeholders (HCEI, PIE).
  • Use data-driven decision frameworks to prioritize evidence gaps and guide research investments for the Dupixent Respiratory portfolio.
  • Contribute to real-world evidence strategies supporting product lifecycle management across the Dupixent Respiratory portfolio.
  • Represent Sanofi at 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 decision-makers to improve HEOR impact and build advocates for Sanofi's respiratory data.
  • Collaborate with external research partners and key opinion leaders to advance E4A strategy and tactical plans for Dupixent in COPD and Asthma.
  • Work with the team lead to engage external evidence bodies (ICER, PDAB, IRA) and apply knowledge of their requirements to evidence generation and value demonstration strategies.
  • Build and maintain working relationships with patient advocacy organizations in respiratory disease.
  • Manage E4A research investments and vendor relationships for assigned indications, ensuring evidence priorities are delivered within budget.
  • Operate independently with minimal supervision, applying scientific and strategic judgment to design and prioritize HEOR activities.
  • Mentor junior E4A team members case-by-case in respiratory HEOR methods, US payer dynamics, and evidence-generation best practices.
  • Develop peer relationships across E4A and cross-functional teams to establish E4A as a center of excellence in Dupixent Respiratory HEOR.
  • Anticipate cross-functional communication needs and address issues through timely action.
  • Contribute to continuous improvement of E4A processes, tools, and capabilities within the Dupixent Respiratory franchise.
  • Apply knowledge of global and US-specific HTA processes and guidelines, and ensure HEOR activities comply with internal SOPs and external laws and regulations.
  • Stay current with US payer policies, formulary management practices, and outcomes-based contracting frameworks relevant to respiratory biologics and COPD and Asthma treatment.
  • Apply HEOR-relevant digital tools and data platforms to improve evidence-generation efficiency and quality.
  • Use digital and AI-enabled solutions to accelerate systematic literature reviews, evidence synthesis, and economic modeling workflows.
  • Understand real-world data analytics and advanced data platforms used in respiratory outcomes research.
  • Maintain foundational knowledge of AI and digital tools relevant to health economics, including data analytics platforms, and develop proficiency with new AI-enabled HEOR solutions.
  • Stay current with emerging digital methodologies relevant to HEOR and champion their adoption within the Dupixent Respiratory E4A team.

Desired Qualifications

  • Experience with HTA submissions is preferred.
  • Prior experience with Dupixent or other respiratory biologics, including familiarity with the clinical evidence base and Dupixent's value story in COPD and Asthma, is strongly preferred.
  • Deep knowledge of the COPD and Asthma competitive landscape, including approved and emerging biologic and non-biologic treatments and their payer positioning in the US market, is preferred.
  • Expertise in Type 2 inflammation biology and its relevance to patient identification, phenotyping, and value demonstration in respiratory disease is preferred.
  • Experience supporting US payer advisory boards, formulary submissions, or outcomes-based contracting negotiations in respiratory disease or biologics is preferred.

About the Company

Sanofi

Global pharma company; vaccines and R&D

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company size
10,001+
Company stage
IPO
Headquarters
Paris, France
Founded
1973

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