About this role
Associate Director, Regulatory Affairs at Nuvation Bio, Inc.. Location: United States or New York or Boston. Role: developing strategy, preparing submissions, managing interactions Requirements: Bachelor's or Master's required, 10+ years regulatory drug development experience, eCTD and submission authoring experience, deep FDA knowledge, ability to travel up to 10%. Category: Legal and Compliance Seniority: Senior Level Tools: eCTD, e-publishing systems Commitment: Full Time Workplace: Hybrid Languages: English