Senior Expert, Regulatory Science — Model-Enabled Development, RWE and Novel Endpoints

Sanofi • Morristown, NJ

43d • Onsite

About The Position

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. As a Senior Manager within our Global specialized Regulatory Science expert unit, you'll play a crucial role in developing innovative regulatory strategies that accelerate drug development through Model-Informed Drug Development (MIDD), Real World Evidence, and novel endpoint approaches. Working directly under Global Head, Regulatory Science — Model-Enabled Development, Real World Evidence & Novel Endpoints, you'll be responsible for hands-on project delivery, regulatory strategy submission, and direct engagement with health authorities on technical matters. This role offers the opportunity to work at the forefront of regulatory science innovation while collaborating closely with Global Regulatory Teams, Translational Medicine, Clinical Development, Biostatistics, and other key R&D functions. You'll contribute to establishing our team as a center of excellence by driving complex regulatory projects, supporting knowledge management initiatives, and helping build specialized capabilities across the organization. This position is ideal for a regulatory professional who thrives on technical challenges and wants to make a direct impact on bringing innovative medicines to patients faster.
About Sanofi: 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.

Requirements

• Bachelor's degree in quantitative science, health science or related field and 5+ years of either pharmaceutical or technology sector industry and/or academia with regulatory affairs experience and demonstrated expertise in drug development and regulatory submissions.
• Proven track record of successful regulatory interactions and submission preparation involving advanced analytical approaches.
• Strong understanding of regulatory frameworks for model-enabled development (e.g., FDA MIDD Pilot Program, EMA modeling and simulation guidance).
• Knowledge of novel endpoint validation processes, biomarker qualification, and real-world evidence regulatory pathways.
• Excellent written and verbal communication skills with the ability to translate complex technical concepts for diverse audiences.
• Proven ability to work effectively in cross-functional teams and build productive working relationships with internal and external stakeholders.
• Strong project management skills with the ability to manage multiple priorities and deliver high-quality work within tight timelines.
• Demonstrated analytical and problem-solving capabilities with attention to detail.
• Ability to work independently while contributing effectively to team objectives.

Nice To Haves

• Direct experience with Model-Informed Drug Development (MIDD), RWE, pharmacometrics, modeling and simulation, or novel endpoint development is highly preferred
• Advanced degree (Masters, PharmD, PhD) in a quantitative science field (e.g., Pharmacometrics, Biostatistics, Pharmacology, Clinical Pharmacology, Computational Biology) or health sciences field preferred.
• Experience with pharmacometric modeling, clinical trial simulation, or endpoint development is highly valued.
• Familiarity with regulatory agency thinking and current trends in regulatory science innovation.
• Experience presenting to regulatory agencies and participating in scientific meetings is preferred.

Responsibilities

• Model-Enabled Regulatory Projects Regulatory Strategies: Lead and validate the regulatory strategies involving MIDD approaches, novel endpoints, and real-world evidence packages. Manage project timelines and deliverables for assigned therapeutic areas / development programs. Collaborate with Global Regulatory Leads (GRLs) to ensure strategies are appropriately integrated into overall projects regulatory plans. Support regulatory validation projects from execution through approval, ensuring alignment with R&D timelines and quality standards.
• Provides Direct Health Authority Engagement and Technical Support: Serve as a technical expert in interactions with regulatory agencies (FDA, EMA, and other global authorities) on modeling, simulation, RWE and novel endpoint topics. Prepare and present technical materials for regulatory meetings, including pre-submission meetings, scientific advice sessions, and advisory committee presentations. Support the development of health authority engagement strategies and maintain productive working relationships with agency reviewers and scientists.
• Drives Cross-Functional Collaboration and Project Delivery: Partner closely with Global Regulatory Teams, Translational Medicine, Clinical Development, Biostatistics, and Medical Affairs teams to ensure regulatory considerations are integrated early in development planning. Facilitate cross-functional working groups and project teams focused on MIDD implementation, RWE and endpoint development. Resolve technical and regulatory issues through collaborative problem-solving and provide regulatory guidance to support optimal study design and data generation strategies.
• Contributes to Knowledge Management and Capability Building: Develop and maintain best practices, standard operating procedures, and training materials for model-enabled regulatory approaches. Support the creation of case studies, lessons learned documents, and knowledge management platforms. Contribute to internal regulatory training programs and capability development initiatives. Monitor regulatory trends and agency guidance documents, providing regular updates to the team and broader organization on emerging opportunities and requirements.
• Supports Regulatory Strategy Development and Risk Assessment: Provide regulatory input and expertise for assigned projects and therapeutic areas, including risk assessment and mitigation planning. Support the development of regulatory strategy frameworks and contribute to strategic decision-making processes. Assist in evaluating new modeling approaches, endpoint technologies, and regulatory pathways for potential implementation across Sanofi's portfolio.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level