About this role
Director, US Regulatory Affairs at Altimmune. Location: Morristown, New Jersey, United States. Role: managing submissions, liaising regulators, developing strategy Requirements: Bachelor's in science/engineering/health with 6+ years regulatory experience in biotech/pharma (or PhD/MD/PharmD with equivalent experience); eCTD submission experience; thorough FDA and global regulatory knowledge; strong project management and communication skills. Category: Research and Development (R&D) Seniority: Senior Level Tools: eCTD Commitment: Full Time Workplace: Hybrid Languages: English