About this role
Associate Director Regulatory Affairs at Viridian Therapeutics, Inc. Location: Waltham, Massachusetts, United States. Role: Represent regulatory, Lead submissions, Prepare submissions Requirements: 10+ years Regulatory Affairs in biopharma; BS in science; experience with INDs/CTAs/NDAs/MAAs; strong regulatory strategy and communication. Category: Research and Development (R&D) Seniority: Senior Level Tools: Microsoft Office, SharePoint Commitment: Full Time Workplace: Onsite Languages: English