Support the Global Regulatory Affairs (GRA) Clinical Trial Application (CTA) manager team in monitoring operational planning and managing CTA documentation
Job Summary
Support the Global Regulatory Affairs (GRA) Clinical Trial Application (CTA) manager team in monitoring operational planning and managing CTA documentation.
Manage activities related to Clinical trials under the European Regulation and its operational processes in the Clinical Trial Information System (CTIS).
Contribute to data quality control, monitor Key Performance Indicators, and prepare appropriate CTA documents in Sanofi repository systems.
Matching Summary
Support the Global Regulatory Affairs (GRA) Clinical Trial Application (CTA) manager team in monitoring operational planning and managing CTA documentation.
Skills & Requirements
Must-have
Clinical Trial Application (CTA) documentation
Clinical Trial Information System (CTIS)
Regulatory document tracking tools
Data quality control and remediation
Monitoring Key Performance Indicators
Nice-to-have
AI-powered research
Cross-functional team collaboration
Patient insights shaping drug development
Work-life balance
Key Requirements
First experience in Regulatory Affairs
Master’s degree in Pharmacy / Science
Fluent English (written and verbal)
European Economic Area citizen aged 18-28
Not a citizen of the country of assignment
Work Rights
European Economic Area citizen aged 18-28, not a citizen of the country of assignment