Director Global Regulatory Affairs Development Pipeline (Oncology) | Pharmacist (m/w/d)

Job Summary

This Director-level role involves acting as the Global Regulatory Lead for assigned oncology development projects, focusing on defining and executing comprehensive regulatory strategies from clinical development through to marketing authorization. Key responsibilities include defining strategies for interactions with national and supranational health authorities (such as the EMA, FDA, and PEI), developing the regulatory storyline for applications and dossiers, and coordinating the preparation and review of essential regulatory documents (e.g., MAAs, IBs). The ideal candidate must possess a university degree in natural sciences (medicine, pharmacy, chemistry, or equivalent) and at least 9 years of relevant regulatory experience, particularly in antibody- and ADC-based cancer therapies. A team-oriented, solution-focused mindset and business fluent English are essential for success in this global, high-impact position.