EU Regulatory Lead, Clinical Affairs - Oncology/ATMPs
Immatics
Immatics is looking for an Associate Director of Regulatory Affairs to enhance the EU Regulatory team. This role involves ownership of EU regulatory strategy for oncology biopharmaceutical programs. You’ll lead regulatory activities, ensuring compliance and strategic alignment within cross-functional teams. The ideal candidate has a Master’s degree in a relevant field, 8+ years of experience in Regulatory Affairs, and a strong capability to manage clinical trial application processes. Join a diverse and motivated team committed to improving cancer treatment. #J-18808-Ljbffr Immatics
Vacancy posted 4 days ago
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