Job Title: RWE Project Lead
Location: Cambridge, MA
Main Responsibilities:Working with 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.
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 actionabe 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 RW Evidence packages
- Ensure proper dissemination and use of study outputs to best support Clinical Development objectives
About You:Main 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 Qualifications:
- Well-developed conceptual thinking skills with capability to access internal and external resources.
- Successful experience working in a global and matrixed environment.
- Excellent communication and influencing skills, with ability to collaborate externally and internally with key customers and stakeholders.
- Strong project management skills and experience.
- Proven leadership and stakeholder management skills.
- Innovative mindset.
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.
- Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
- Help improve the lives of millions of people globally by making drug development quicker and more effective.
- Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
North America Applicants Only
The salary range for this position is:
$148,500.00 - $214,500.00
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.
