About this role
Director/Senior Director, Regulatory Affairs at Tenpoint Therapeutics. Location: United States. Role: leading strategy, managing submissions, leading interactions Requirements: 10+ years regulatory affairs experience in pharma/biotech with NDA and FDA interaction experience; deep CMC knowledge; experience across global regions; strong project management; proficiency with Veeva RIM and MS Office. Category: Research and Development (R&D) Seniority: Senior Level Tools: Veeva RIM, Electronic Medical Records (EMR), Microsoft Excel, Microsoft Word, Microsoft PowerPoint Commitment: Full Time Workplace: Hybrid Languages: English