ph3Global Regulatory Affairs Clinical Trials Coordinator - VIE Contract /h3ulliLocation: Italy, Milano /liliTarget start date: 01/12/2026 /li /ulpiMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. /ppPLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship. /ppPLEASE 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. /ph3About the job /h3pAs Global Regulatory Affairs Clinical Trials Coordinator VIE within our Global Regulatory Affairs team, you’ll manage regulatory activities related to Clinical Trials Applications, from planning and dossier preparation, then submission, responses to Health Authorities and approvals of Trials. We are developing our knowledge in Clinical Trial Applications (CTA) related Intelligence, in particular our knowledge in the European Clinical Trial Regulation. Your work will support knowledge development, and field experience for the European Clinical Trial Regulation processes. /ppJoin the engine of Sanofi’s mission - where deep immunoscience meets bold, AI-powered research. In RD, you’ll drive breakthroughs that could turn the impossible into possible for millions. /ppReady to get started? /ph3About Sanofi /h3pWe’re an RD-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. /ph3Main responsibilities: /h3ulliProvide regulatory expertise to Sanofi key stakeholders and help teams understand and follow important healthcare regulations. /liliSet up processes and coordinate the preparation of Clinical Trial Applications (CTAs). /liliWork closely with different departments including Research Development (RD), Clinical Operations, and Pharmacovigilance teams. /liliEnsure all documentation meets quality standards. /liliMonitor the Progress of CTAs through submission and approval stages. /liliIdentify potential issues early and develop practical solutions, keep projects moving forward on schedule and drive process improvement. /liliHelp implement new regulatory processes (Clinical Trial Regulation in Europe, EU Clinical Data Disclosure). /liliContribute to developing more efficient ways of working, stay current with changing regulations and help teams adapt. /li /ulh3About you /h3h3Experience: /h3ulliPrevious experience in pharmaceutical industry in Regulatory Affairs or similar field. /liliClinical Trial Regulations experience is highly preferred. /li /ulh3Soft and technical skills: /h3ulliGood communication negotiation skills. /liliProactiveness, and problem-solving ability. /liliAbility to work with cross-functional teams. /liliAbility to handle multiple tasks and projects simultaneously. /li /ulh3Education: /h3ulliMaster's Degree in Pharmacy,



or other relevant scientific field. /li /ulh3Languages: /h3ulliFluency in English (written and verbal). /liliItalian knowledge would be an asset. /li /ulh3Why choose us? /h3ulliBe part of a pioneering biopharma company where patient insights shape drug development. /liliWork at the forefront of AI-powered science that accelerates discovery and improves outcomes. /liliCollaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams. /liliHelp improve the lives of millions of people globally by making drug development quicker and more effective. /liliEnjoy 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. /liliJoin a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice. /liliAchieve genuine work-life balance in a supportive RD environment. /li /ulpiMove 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. /ppSanofi’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. /pp#LI-EUR /p /p #J-18808-Ljbffr

📌 Global Regulatory Affairs Clinical Trials Coordinator VIE Contract (Milano)
🏢 Sanofi
📍 Milano