Clinical Development RWE Project Lead (CDRPL)
Cambridge, Massachusetts Permanent Posted on Mar. 07, 2025 Closing on Jul. 06, 2025Job title: Clinical Development RWE Project Lead (CDRPL)
Location: Cambridge, MA
About the Job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
Reporting to the 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.
They will 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 are fulfilled.
The CDRPL will execute the project-specific roadmap to ensure successful delivery of the project.
They will highlight and execute portfolio strategies to source data needed for GPT's project deliverables.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
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 TAs.
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 RWE packages
Ensure proper dissemination and use of study outputs to best support Clinical Development objectives
About You
Requirements
Degree in Epidemiology, Biostats or equivalent scientific discipline
MS with a minimum of 3+ years or BS with a minimum of 5+ years experience working in operational RWE role(s)
Expertise with current techniques in data analysis, digital and AI/ML
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 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.
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Pursue progress. Discover extraordinary.
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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com
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