Real World Evidence Scientific Lead

Sanofi•Morristown, NJ

1d•$178,500 - $257,833•Hybrid

About The Position

The Real-World Data & Evidence Science (RWD&ES) team, in General Medicines Medical, serves as an end-to-end strategy and execution partner to solve business problems using real-world data. We partner with cross functional partners to lead end-to-end the planning and execution of real-world evidence (RWE) strategies. 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. Sanofi is 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.

Requirements

Advanced degree in pharmaco-epidemiology, biostatistics, or Health Outcomes (PhD preferred).
Minimum 5 years in real-world evidence (RWE) generation for pharmaceutical industry with end to end leadership experience
Strong publication track record in relevant journals.
Experience across therapeutic areas, including transplant, diabetes, and cardiovascular.
Ability to influence and motivate teams as well as senior leaders.
Strategic thinking for innovative evidence generation.
Urgency, ownership, and proactive attitude.
Expertise in pharmacoepidemiology, HEOR, and RWE study design.
Working with routinely collected healthcare data.
End-to-end project management for real-world studies.
Understanding of commercial strategy.
Fluent English is mandatory.

Nice To Haves

Education in business is a plus.
a second European language is appreciated.

Responsibilities

Manage the implementation of cutting-edge, effective, and efficient real world evidence strategy for the development of autoimmune type 1 diabetes (aT1D).
Manage the end-to-end planning, execution and communication of specific research studies, ensuring that deliverables are on time, within budget, to specification and of high scientific rigor that demonstrates commitment to quality.
Deliver strategic scientific input in all stages of RWE study conceptualization through study closure, including study design, cohort construction, protocol & statistical analysis plan development, study operations, data analysis, results interpretation and clinical study report development.
Collaborate with cross-functional stakeholders and relevant internal and external scientific experts based on specific needs of individual RWE studies to ensure that the real-world data and RWE generation is fit-for-purpose to the intended use, whether for regulatory, market access or clinical use.
Serve as methodological expert in the design and execution of real-world study plans to address critical evidence generation gaps as well as in-house study methodology expert leveraging opportunities to use innovative RWE study designs and analytics to deliver on critical needs.
Identify and validate external fit-for-purpose data sources, associated institutions and/or organizations, in collaboration with other members of the RWD&ES team.
Manage the development of budgets for RWE studies in collaboration with relevant internal and external stakeholders, including RWE Operations, Sanofi Global Hub and/or vendors as appropriate, to support the annual strategic and budget planning process and periodic updates.
Maintain timely communication and close alignment with team members, partners and stakeholders to ensure clear and timely visibility the evidence strategy, study progress and anticipation of challenges and risk mitigation.
Accountable for supporting GenMed medical gaps within the Global Integrated Evidence Generation Plans (IEGP).