About this role
Larimar Therapeutics - Director, Regulatory Affairs, Ex-US at Larimar Therapeutics. Location: Philadelphia, Pennsylvania, United States. Role: lead submissions, develop strategy, collaborate stakeholders Requirements: 4+ year undergraduate degree; 5–8 years in regulatory affairs; EMA/MHRA experience preferred; global submissions experience; strong communication and project management. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Onsite Languages: English