Jobs at Larimar Therapeutics, Inc.

The Senior Manager, Trial Master File Management oversees study-specific TMFs, ensures compliance with regulations, manages vendors, and leads TMF training and improvements.

The Director, Regulatory Affairs will lead global regulatory strategies and activities, ensure compliance, and collaborate with project teams for product development in various global regions.

Oversee GxP computerized systems implementation, compliance, and support for clinical and commercial operations, ensuring adherence to regulatory standards.

The National Sales Director will lead the U.S. launch of nomlabofusp, develop national sales strategies, build a high-performing team, and ensure compliance in sales activities while engaging key stakeholders.

The Director, Business Development will strategize and execute on partnerships while managing relationships, conducting market analysis, and providing strategic guidance to leadership.

The Director, Quality will manage Larimar's Quality Management System, ensuring compliance with GCP/GCLP/GVP guidelines, support inspections, and improve quality standards.

The Director of Data Management leads clinical data management, ensuring operational excellence and compliance with regulatory standards while driving collaboration across departments and improving processes.