About this role
Director, Global Regulatory Affairs at Protara Therapeutics, Inc.. Location: New York or United States. Role: lead submissions, interpret feedback, coordinate teams Requirements: MD/PhD/PharmD with 10+ years of regulatory affairs in biopharma; ex-US submissions; IND/CTA leadership; strong communication and project management. Category: Research and Development (R&D) Seniority: Senior Level Tools: MS Office, NetSuite, Workday Adaptive Planning, Smartsheet Commitment: Full Time Workplace: Hybrid Languages: English