About this role
Associate Director, Regulatory Affairs Operations at Merida Biosciences. Location: Cambridge, Massachusetts, United States. Role: managing submissions, coordinating timelines, maintaining documentation Requirements: Bachelors in life sciences required; 7+ years regulatory affairs/operations experience in pharma/biotech; experience with RIMS/EDMS/Veeva Vault, eCTD, project planning tools and Microsoft Office; knowledge of FDA/EMA/ICH standards. Category: Research and Development (R&D) Seniority: Senior Level Tools: RIMS, EDMS, Veeva Vault Regulatory, eCTD, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams, Smartsheet, Microsoft Project Certifications: pmp Commitment: Full Time Workplace: Onsite Languages: English