Junior Project Manager - VIE Contract

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