About this role
Associate Director, Clinical Compliance & Records at Amylyx Pharmaceuticals. Location: Cambridge, Massachusetts, United States. Role: ensuring compliance, managing TMF, supporting inspections Requirements: Bachelor's in a health/science field, 8+ years pharma/biotech clinical compliance or TMF experience, ICH/GCP knowledge, Veeva/eTMF and MS Office proficiency, strong communication and organizational skills. Category: Legal and Compliance Seniority: Senior Level Tools: Veeva Clinical, Veeva Quality, TMF Reference Model, Microsoft Word, Microsoft Excel, Microsoft SharePoint, Microsoft PowerPoint Commitment: Full Time Workplace: Hybrid Languages: English