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RWE Project Lead

Job in Cambridge, Middlesex County, Massachusetts, 02141, USA
Listing for: Sanofi
Full Time position
Listed on 2026-08-06
Job specializations:
  • IT/Tech
    AI Engineer (Applied/Software), Data Science Manager, Data Analyst
Job Description & How to Apply Below

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.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions.

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
  • Working with Clinical Development RWE Portfolio Heads, the Clinical Development RWE Project Lead (CDRPL) will work at project level within specific TAs and across functions to lead high-impact projects, leveraging core RWE AI evidence generation platforms and other RWE assets, based on clinical development needs and current/future pipeline.
  • The CDRPL will drive RWE projects prioritized by Clinical Development RWE Portfolio Heads, based on evidence needs for clinical development and current/future molecule pipeline, by leveraging one of the core RWE evidence generation platforms.
  • He/She will also work in close contact with other internal partners such as Global Project Team (GPT) members, Clinical Science Organization, Research, Digital Office and Global Regulatory teams to ensure the needs and ambitions of TAs and assets are fulfilled.
  • The CDRPL will execute the project-specific roadmap to ensure successful delivery of the project.
  • He/She will have to bring value by bringing to GPTs project deliverables, highlight and execute portfolio strategies to source data needed to run projects.
Focusing Efforts In The Following Areas

Delivery of RWE evidence generation projects for relevant therapeutic areas

  • Lead multidisciplinary teams, ensuring effective project execution plan and timelines.
  • Coordinate with RWE portfolio Heads, GPTs and other key stakeholders to design project minimum viable product: identify, understand and address user needs, ensuring alignment among stakeholders and translating them into actionable project goals and deliverables.
  • Create project business cases, document and report project activities and define system requirements and dependencies with other projects.

Contribution to RWE portfolio and platforms strategy within relevant therapeutic areas

  • Inform roadmap for the RWE platform projects by overseeing the end-to-end development of project and dependencies
  • Ensure access modalities to fit-for-purpose datasets, in collaboration with relevant Sanofi stakeholders in relevant TA's.
  • Have external facing interactions to drive adoption of RWE in clinical development, at FDA/EMA level.

Interact with external policy groups in collaboration with Regulatory function

  • Generate/discuss regulatory and other RW Evidence packages
  • Ensure proper dissemination and use of study outputs to best support Clinical Development objectives
About You

Basic Qualifications:

  • PhD, or MSc, in Health Sciences with quantitative background, Epidemiology or Public Health.
  • Minimum 2 years of previous experience in Real Word/clinical project in industry required.
  • Proven capability to deliver complex projects.
  • Understanding of TA relevant to Sanofi context (such as I&I, Neuroscience or rare diseases), current needs and latest innovations in clinical development and evidence generation.
  • Understanding of RWE, data analytics and statistics.
  • Understanding of legal and regulatory environment influencing clinical development plans, labelling and promotional claim. Past experience / excitement around big data / modern tech stack environment.

Preferred…

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