Global Regulatory Affairs Director - Late-Phase Lead

A clinical-stage biopharmaceutical company is seeking a Director, Regulatory Affairs to lead global regulatory efforts for a multi-indication late-phase investigational product. You will oversee regulatory submissions in the US and EU, contribute to clinical development, and guide the team on regulatory strategies. The ideal candidate will have over 10 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry, strong leadership skills, and a detail-oriented approach to problem-solving. #J-18808-Ljbffr