Director, Regulatory Affairs — US NDA Lead (Oncology)

A clinical-stage precision oncology company is seeking a Director of Regulatory Affairs to lead the preparation and execution of NDA filings for late-stage oncology programs. This pivotal role requires a minimum of 12 years in the pharmaceutical/biotech industry and 8 years in Regulatory Affairs, with proven success in US NDAs. Strong leadership and communication skills are essential for coordinating cross-functional teams and driving regulatory strategies. A comprehensive understanding of oncology drug development is paramount, along with a degree in a relevant field. #J-18808-Ljbffr