About this role
Associate Director, Regulatory Affairs Project Management at Insmed. Location: Bridgewater, New Jersey, United States. Role: leading submissions, coordinating submissions, managing projects Requirements: Bachelor's (life sciences or chemistry preferred),7+ years regulatory affairs experience,project management in pharma,knowledge of global regulatory submissions and eCTD,experience with Veeva Vault RIM,Smartsheet,and Microsoft Office. Category: Project and Program Management Seniority: Senior Level Tools: Veeva Vault RIM, Smartsheet, Microsoft Office, eCTD Commitment: Full Time Workplace: Remote Languages: English