Global Regulatory Affairs Clinical Trials Coordinator VIE Contract
Global Regulatory Affairs Clinical Trials Coordinator - VIE Contract
- Location: Italy, Milano
- Target start date: 01/12/2026
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
Main responsibilities
- Provide regulatory expertise to Sanofi key stakeholders and help teams understand and follow important healthcare regulations.
- Set up processes and coordinate the preparation of Clinical Trial Applications (CTAs).
- Work closely with different departments including Research & Development (R&D), Clinical Operations, and Pharmacovigilance teams.
- Ensure all documentation meets quality standards.
- Monitor the Progress of CTAs through submission and approval stages.
- Identify potential issues early and develop practical solutions, keep projects moving forward on schedule and drive process improvement.
- Help implement new regulatory processes (Clinical Trial Regulation in Europe, EU Clinical Data Disclosure).
- Contribute to developing more efficient ways of working, stay current with changing regulations and help teams adapt.
About you
Experience:
- Previous experience in pharmaceutical industry in Regulatory Affairs or similar field.
- Clinical Trial Regulations experience is highly preferred.
Soft and technical skills
- Good communication & negotiation skills.
- Proactiveness, and problem-solving ability.
- Ability to work with cross-functional teams.
- Ability to handle multiple tasks and projects simultaneously.
Education
- Master's Degree in Pharmacy, or other relevant scientific field.
Languages
:
- Fluency in English (written and verbal).
- Italian knowledge would be an asset.
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.
- Achieve genuine work-life balance in a supportive R&D environment.
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
Not included in the source posting: benefits.
Skills
Who can apply
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