Description
Amgen is hiring a Biostatistical Programming Senior Associate to support complex clinical trial data analysis and regulatory submissions. The role involves SAS and/or R programming, SDTM and ADaM dataset creation and validation, statistical programming specifications, regulatory documentation, data quality checks, and collaboration with global study teams. The position is based in Hyderabad, India, and requires a relevant degree plus at least four years of statistical programming experience in a clinical development environment, along with strong CDISC, SAS, data quality, and English communication skills.
