Associate Director, Clinical Data Programmer

Role: Associate Director, Clinical Data Programming at Amylyx, leading technical data management support for clinical trials. Responsibilities: manage EDC platforms (Medidata RAVE), develop and validate clinical databases, ensure data integrity and compliance with CDISC standards, lead system design, validation, and UAT; develop SAS macros and visualizations; oversee external vendor quality and support cross-functional teams in data insights and problem-solving. Requirements: Bachelor’s in Life Science or related; 8+ years in clinical data management with extensive SAS, R, or Python experience; expertise in Medidata RAVE, CDISC standards (CDASH, SDTM), and data visualization tools. Preferred: experience creating advanced data visualizations using SAS, R, Python, Power BI, Tableau, or Spotfire. High-Value: clinical-stage biotech environment, focus on rare and high unmet need diseases, remote work with periodic travel to Cambridge, MA; salary range $188K–$211K.