About this role
Director, Regulatory CMC at Iovance Biotherapeutics. Location: United States. Role: leading teams, preparing applications, negotiating strategy Requirements: BS in life sciences, 10+ years regulatory affairs experience with late-stage oncology drug development, strong regulatory strategy, submission and health authority interaction skills, excellent writing and project management. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Remote Languages: English