About this role
Associate Director, Regulatory Affairs at Iovance Biotherapeutics. Location: United States. Role: leading programs, preparing submissions, negotiating submissions Requirements: 10+ years regulatory affairs experience (Bachelor\u0002s) or 8 years (Master\u0002s) or 5+ years (PhD); BS in life sciences required; late-stage oncology and global regulatory experience; strong writing, negotiation, and project management skills. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Remote Languages: English