Overview
Role involves leading regulatory strategies and activities for late-stage gene therapy programs.
Ideal candidate has 7+ years of regulatory experience with strong knowledge of EMA and EU/UK regulations.
hybridseniorfull-timeEnglish
Locations
United Kingdom, England, London
Requirements
Minimum 7 years regulatory experience Strong knowledge of EMA and EU/UK regulations Experience in regulatory submission project management
Responsibilities
Lead EU/UK regulatory activities Manage submissions to regulatory authorities Coordinate with global teams for alignment