Associate Director, Clinical Data Programmer

Role: Associate Director, Clinical Data Programming at Amylyx, providing technical leadership and hands-on support for clinical data management in early-phase trials. Responsibilities: serve as SME for Medidata RAVE EDC platform, oversee system development, validation, and compliance; develop data programs including SAS macros, listings, and visualizations; support data collection, database lock, and vendor oversight; ensure adherence to CDISC standards and regulatory requirements; collaborate across Clinical Data Management, Biostatistics, and Operations. Requirements: Bachelor's in Life Science or related; 8+ years in clinical data management with extensive experience in Medidata RAVE, SAS, R, or Python; knowledge of CDISC standards (CDASH, SDTM); proficiency in data visualization tools (SAS, R, Power BI, Tableau); strong organizational, communication, and multi-project management skills. HighValue: clinical stage, early-phase trials, focus on post-bariatric hypoglycemia, Wolfram syndrome, ALS; GxP, ICH, 21 CFR Part 11 compliance; remote work within the US with periodic travel to Cambridge, MA. Work setup: remote, US-based; travel required.