Associate Director, Eucan Regulatory Lead - Oncology
Takeda UK
Zurich, Switzerland
Fully remote
Eucan regulatory strategy
Late-phase oncology asset
Development-to-approval continuum
Define, develop, and lead the regional regulatory strategy within the EUCAN region for a key late-phase oncology asset with multiple indications
Job Summary
Define, develop, and lead the regional regulatory strategy within the EUCAN region for a key late-phase oncology asset with multiple indications.
Support regulatory activities across the development-to-approval continuum, including planning, preparation, and timely approval of investigational submissions through marketing authorization applications and lifecycle management.
Lead interactions with health authorities in the region and represent Takeda in Health Authority meetings.
Matching Summary
Define, develop, and lead the regional regulatory strategy within the EUCAN region for a key late-phase oncology asset with multiple indications.
Skills & Requirements
Must-have
EUCAN regulatory strategy
late-phase oncology asset
development-to-approval continuum
interactions with health authorities
regulatory submissions and approvals
Nice-to-have
advanced therapeutic medical products
value and access team support
new business development evaluation
Key Requirements
BSc or advanced scientific degree
Minimum 8 years of experience in drug regulatory affairs
Experience with advanced therapeutic medical products advantageous
Solid regulatory experience in EU/GEM region
Experience leading interactions with Health Authorities