About this role
Director of Regulatory Affairs at Avalo Therapeutics. Location: Chesterbrook, Pennsylvania, United States. Role: leading strategy, providing guidance, submitting documents Requirements: 10–15 years regulatory affairs experience in biotech/pharma, bachelor's degree required (advanced degree preferred), experience with late-stage and biologics development, FDA interactions, and managing CROs/consultants. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Onsite Languages: English