Junior Project Manager - VIE Contract at Sanofi in Cambridge, MA

Junior Project Manager - VIE Contract Location: Cambridge, MA Junior Project Manager - VIE Contract Location: United States of America, Cambridge Target start date: 01/10/2026 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 Junior Project Manager VIE within our Development Global Project Management team, you’ll apply and grow your project management foundations in clinical development across a dynamic, evolving portfolio. Therapeutic area expertise will be developed during the assignment — the successful candidate brings the project management toolkit; disease area knowledge will be built through structured mentorship, immersive team participation, and dedicated learning. The role carries a dual scope: 1. Assigned Therapeutic Area(s): Applying existing clinical development project management skills to support global project management activities across assigned programs within the portfolio, while progressively building therapeutic area expertise through mentorship, training, and hands-on experience within established Global Project Teams (GPTs). 2. Evolving Disease Area Activities: Contributing as a GPM to emerging or evolving disease area programs, leveraging transferable project management skills to provide cross-functional coordination and project management support as Sanofi's portfolio priorities develop over the course of the assignment. ​​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: Scientific & Technical Contribution Leverage existing clinical development knowledge to contribute meaningfully to program discussions from day one, while actively building therapeutic area expertise across assigned disease areas throughout the assignment. Engage proactively with scientific literature, competitive intelligence, and disease area landscape materials to accelerate therapeutic area learning. Contribute to the preparation and review of key program documents, including Target Product Profiles (TPPs), development plans, and regulatory strategy documents — applying transferable skills from prior clinical development experience. Support the integration of input from cross-functional platforms (clinical, regulatory, CMC, translational medicine, statistics, safety) to ensure alignment with agreed clinical plans. Progressively develop the ability to critically evaluate scientific and clinical data specific to assigned therapeutic and disease areas as the assignment advances. Project Management & Coordination Apply established project management skills to support the development and maintenance of global project plans across assigned portfolio programs. Coordinate cross-functional activities within the GPT, ensuring deliverables are tracked and escalated appropriately — drawing on prior experience in clinical development environments. Assist in the preparation of materials for internal governance bodies, decision boards, and alliance committees and support the preparation of regulatory documents, responses to Health Authority questions, and labeling-related activities under the guidance of senior GPMs and the GPM Head. Cross-Functional & Stakeholder Engagement Actively participate in Global Project Team (GPT) meetings, contributing to discussions and capturing action items and decisions. Support management and coordination of interactions with external stakeholders, including regulatory authorities, key opinion leaders, advisory boards, and patient advocacy groups, under senior supervision, and collaborate with Market Access, Global Commercial, and Medical Affairs teams as part of the GPT. Contribute to publication strategy and communication plans in coordination with Medical Affairs and Commercial teams. Support alliance partner coordination activities where applicable, ensuring program strategic alignment. Build therapeutic area networks within assigned disease area communities — including internal subject matter experts, external collaborators, and key opinion leaders — as a core development objective of the assignment. Evolving Disease Area Activities Help establish project governance frameworks, timelines, and cross-functional coordination processes for new or developing disease area teams. Bring a fresh perspective and proactive mindset to support the strategic development of Sanofi's expanding and evolving disease area portfolio. Adapt fluidly to shifting portfolio priorities, demonstrating versatility across therapeutic contexts over the course of the assignment. About you Experience: At least 1 year full-time work experience in clinical development project management, across any therapeutic area. Soft and technical skills: Strong interpersonal and communication skills; ability to work effectively in multicultural, international environments. Demonstrated ability to synthesize complex scientific and operational information and to work in a structured, organized, and detail-oriented manner. Proactive, curious, and solutions-oriented mindset with a genuine interest in expanding therapeutic area expertise across a dynamic portfolio. Demonstrated ability to coordinate cross-functional activities, track deliverables, and manage timelines in a clinical or pharmaceutical development context. Strong scientific curiosity and willingness to rapidly develop expertise across new therapeutic and disease areas. Comfort working across multiple disease area contexts, in a matrixed organization with multiple stakeholders and evolving priorities. Familiarity with drug development processes (clinical trials, regulatory submissions, CMC). Education: Master's Degree in Life Sciences, Pharmacy, Medicine, Biomedical Engineering, or a related scientific discipline. Languages: Fluent in English (verbal and written). Additional European language skills are a plus. 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 sanofi.com! US and Puerto Rico Residents Only Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.