Associate Director, Eucan Regulatory Lead - Oncology
Takeda
Zurich, Switzerland
Fully remote
Eucan regulatory strategy
Late-phase oncology asset
Development-to-approval continuum
Takeda is seeking an Associate Director to lead EUCAN regulatory strategies for its oncology portfolio, focusing on the development and approval of late-phase oncology assets. The role involves collaborating with senior regulatory leads and health authorities to ensure timely approvals and effective lifecycle management of products
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 future marketing authorization applications and ongoing lifecycle management.
Lead interactions with health authorities in the region for an asset and may support value and access team in their interactions with Health Technology Assessment (HTA) bodies for products within their responsibility.
Matching Summary
Match Score: 85
Takeda is seeking an Associate Director to lead EUCAN regulatory strategies for its oncology portfolio, focusing on the development and approval of late-phase oncology assets. The role involves collaborating with senior regulatory leads and health authorities to ensure timely approvals and effective lifecycle management of products.
Skills & Requirements
Must-have
EUCAN regulatory strategy
late-phase oncology asset
development-to-approval continuum
interactions with health authorities
regional regulatory submissions
Nice-to-have
advanced therapeutic medical products experience
value and access team support
new business development evaluation
inclusive culture promotion
Key Requirements
BSc. Advanced scientific related degree preferred
Minimum of 8 years of experience in drug regulatory affairs