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Sanofi

Global pharma company; vaccines and R&D

Evidence Synthesis Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listed

About the Job

Requirements

  • At least 8 years of experience in HEOR for the pharmaceuticals industry, CRO consultancy, or academia.
  • Demonstrated effective communication, organizational, and interpersonal skills; ability to work effectively as part of multidisciplinary global teams and independently within management direction, functional policies, budgetary guidelines, company values, ethics, and applicable law; ability to handle multiple projects across different therapeutic areas; understanding of the disease environment and the evolution of the market access landscape and its business implications; successful experience in a project- or matrix-oriented environment; ability to present complex information clearly to internal and external audiences; team spirit, multicultural awareness, and ability to drive matrix teams.
  • Strong analytical skills to translate clinical and economic information into payer evidence strategies.
  • Understanding of reimbursement decisions, value drivers, and how evidence is used in decision-making and affects providers, patients, and health systems.
  • Knowledge of health economics and health technology assessment (HTA) review methods and principles.
  • Advanced degree in life sciences, pharmacy, a similar discipline, or medical degree.
  • Excellent spoken and written English.

Responsibilities

  • Manage assigned Evidence Synthesis projects in the portfolio, planning and generating robust health economics and value-based evidence to maximize value propositions from global and US perspectives in collaboration with Global HEVA business partners and the Global HEVA Evidence Synthesis lead.
  • Manage and execute quality research projects, economic models, trial design recommendations, and other activities supporting programs and products.
  • Support planning, design, implementation, and completion of innovative evidence-based research programs aligned with program and product strategies, producing evidence and tools for internal decision-making and external audiences at product launch and throughout the product life cycle.
  • Identify opportunities to innovate HEVA value identification, evidence generation, and dissemination processes and plans to improve the relevance and impact of evidence and support optimal reimbursement and access decisions.
  • Create complex, specialized strategic content without supervision; develop and maintain therapeutic-area expertise; develop and review content created by HEVA associates; and coach HEVA associates.
  • Develop and maintain effective relationships with Medical Affairs, Clinical Development, Commercial, and Market Access stakeholders; provide feedback to HEVA associates to develop their knowledge and share expertise; and work with global HEVA teams across time zones.
  • Manage HEVA evidence-generation projects with Global HEVA business partners by developing research plans for pre-launch, launch, and post-launch evidence for investigational and marketed drugs. Plans include burden-of-illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and development and analysis of patient-reported outcomes.
  • Work with HEVA product leads to manage and execute research studies supporting the clinical, economic, and humanistic value of products.
  • Lead development of core value dossiers (CVD) and AMCP dossiers under the strategic direction of Global HEVA business partners.
  • Develop complex HEVA strategic evidence materials and build expertise in the assigned therapeutic area.
  • Manage core HEVA strategic evidence-generation processes, templates, and products across the portfolio in accordance with scientific and value messages aligned with the CVD, US AMCP dossier, and HEVA contributions to other submissions.
  • Ensure adherence to evidence-generation guidelines and other standards relevant to HEVA processes at SBO.
  • Use advanced training-delivery tools and techniques; design action plans based on end-customer feedback and improve course content and delivery.
  • Work with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs, and Market Access teams to identify evidence-generation and dissemination needs and develop assigned deliverables.
  • Prepare relevant, customized deliverables with stakeholder teams and ensure assigned project milestones and timelines remain on track.

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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