Global Regulatory Submission Lead

Excelya is seeking a Global Regulatory Submission Manager Consultant to lead and coordinate regulatory submission activities across the product lifecycle, from FIH development through post-approval maintenance and license withdrawal.

In this senior role, you will drive planning and execution across FDA, Europe, China, and Japan, ensuring high-quality dossiers delivered on time and compliant with global requirements, working closely with Medical Writing, Clinical Development, and R&D Operations.