Clinical Trial Coordinator - VIE contract
Synthorx
Clinical Trial Coordinator - VIE Contract
- Location: Hungary, Budapest
- Target start date: 01/07/2026
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 Clinical Trial Coordinator VIE within our Regulatory Affairs team, you will support the Global Regulatory Affairs (GRA) Clinical Trial Application (CTA) manager team, to follow up/monitoring of CTA operational planning activities, manage activities related to CTA documentation in close collaboration with the Clinical trial team, and the Regulatory team.
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:
- Follow up/monitoring of Clinical Trial Application (CTA) operational planning activities.
- Manage activities related to CTA documentation in close collaboration with the Clinical trial team, and the Regulatory team (coordinate, follow, check availability of component and completeness of CTA dossier and ensure availability of documents for Initial Clinical Trial Applications (CTA) preparation, CTA amendments, etc.).
- Manage activities specifically related to the Clinical trials under the European Regulation and its operational processes in the Clinical Trial Information System (CTIS).
- Prepare appropriate CTA documents in the Sanofi repository systems.
- Activities related to Development Safety Update Report (DSUR) delivery.
- Manage activities related to tools /Sanofi Regulatory document and registration tracking tools (Vault RIM).
- Contribute to data quality control, and appropriate data remediation in Vault RIM.
- Monitor Key Performance Indicators by running reports, collating data and report as per oversight and governance process.
About you
Experience:
- First experience in Regulatory Affairs or other relevant experience.
Soft and Technical skills:
- Good communication skills.
- Good negotiation skills.
- Ability to solve issue & pro-active behaviour.
- Ability to work with multi-function teams.
- Ability to manage multiple projects.
Education:
- Master’s degree in Pharmacy / Science or other related degree.
Languages:
- Fluent English (written and verbal).
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.
- Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
- 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.
- 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.
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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!