Portfolio Strategy Associate VIE Contract

Portfolio Strategy Associate - VIE Contract Location: United States of America, Morristown Target start date: 01/01/2027 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship. PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address. About the job As Portfolio Strategy Associate VIE within Global Regulatory Portfolio Strategy & Innovation team, you’ll play a key role in supporting the evolution of our Blueprint model. Blueprint is GRA’s approach to developing regulatory strategies with the ambition to achieve ONE Regulatory voice and deliver well-differentiated, value-added, sustainable products with competitive product labels. In this role, you will support the development, maintenance, and deployment of the Blueprint framework, helping to strengthen our operating model, simplify ways of working, and ensure alignment across processes, governance, templates, and roles & responsibilities. You will work closely with key stakeholders across GRA, gaining exposure to global regulatory strategy, organizational design, and transformation at scale. 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. Ready to get started? 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. Main responsibilities: GRA Blueprint Model Support & Enhancement Support the deployment and continuous improvement of the GRA Blueprint Model across US-based regulatory teams, ensuring consistent adoption and effective use. Contribute to Blueprint model evolution by gathering user feedback, documenting lessons learned, and identifying opportunities for optimization. Assist in the development and delivery of Blueprint training materials and onboarding programs for new users. Project Risk Management & PRS Implementation Support GRA project risk management capability building by coordinating training sessions and providing user support for the R&D project risk management tool. Assist in quality control of risk data migration and new risk entries to ensure consistency and completeness. Support the end-to-end PRS (Probability of Regulatory Success) process implementation, including data collection, analysis, and reporting. Contribute to transparent PRS tracking from team proposals through governance endorsement. Digital Transformation & AI Integration Coordinate with regulatory Subject Matter Experts (SMEs) to gather requirements and feedback for TRACY (Trusted Regulatory AI Companion for You) and other digital initiatives. Support testing cycles and user acceptance activities for regulatory digital tools. Help identify opportunities for process digitalization and automation within Portfolio Strategy workflows. Strategic Communication & Stakeholder Engagement Assist in coordinating the GRT and GRA Strategy & Innovation Forum, including logistics, content preparation, and follow-up actions. Help prepare presentations, reports, and communications for TPSC meetings and other governance forums. Maintain documentation repositories and ensure information is accessible and up-to-date. About you Experience: At least 1-year full time experience working in the pharmaceutical /biotechnology industry. Experience with project coordination or cross-functional team collaboration. Exposure to regulatory affairs, drug development, or related R&D functions is a plus. Soft and technical skills: Proficient with Microsoft Office 365 suite (Word, Excel, PowerPoint, Teams). Familiarity with SharePoint and collaborative digital platforms. Interest in AI/digital tools and regulatory data platforms. Strong analytical skills with attention to detail and data accuracy. Ability to quickly learn new software tools and systems. Excellent organizational and time management skills with ability to handle multiple priorities. Strong written and verbal communication skills, with ability to synthesize complex information. Proactive, self-motivated, and able to work autonomously in a matrixed environment. Collaborative mindset with ability to build relationships across cultures and geographies. Adaptable and comfortable with ambiguity in a fast-paced, changing environment. Intellectual curiosity and eagerness to learn about regulatory strategy and drug development. Education: Master's degree in Life Sciences, Pharmacy, Regulatory Affairs, or related scientific discipline. Languages: Fluent English (verbal and written). Why choose us? Be part of a pioneering biopharma company where patient insights shape drug development. Work at the forefront of AI-powered science that accelerates discovery and improves outcomes. Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams. Help improve the lives of millions of people globally by making drug development quicker and more effective. Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs. Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice. iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow. Sanofi’s Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work. #LI-EUR 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, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at ! US and Puerto Rico Residents Only Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.