About this role
Director, Regulatory Affairs at Eikon Therapeutics. Location: Jersey City, New Jersey, United States. Role: Lead submissions, Develop strategy, Collaborate cross-functional Requirements: 10+ years regulatory affairs experience; FDA and international regulatory knowledge; clinical regulatory content and submissions; strong communication; individual contributor. Category: Research and Development (R&D) Seniority: Senior Level Tools: eCTD, Regulatory submissions Commitment: Full Time Workplace: Hybrid Languages: English