Sr Stat Prog Analyst

Candidates will provide SAS and other programming support with respect to design, conduct & analysis of clinical trials; participate in clinical trial process by reviewing protocols, CRFs, data management and statistical analysis plans, generate statistical analysis data sets, and produce summary tables, listings and graphs for individual studies as well as for NDAs (ISS,ISE); oversee and coordinate CRO programming activities; and manage programming activities involving NDAs. A minimum of 5 years of experience using SAS in a biomedical or other health related field is required, with a minimum of 3 years of experience directly related to NDAs. Experience in extracting clinical data from Oracle Clinical relational data base, and using SAS in a UNIX OS environment are preferred. Candidates must have extensive knowledge of SAS, SAS GRAPH, and MACROs; have excellent validation and documentation skills, and experience in extracting data from databases and creating analysis files based on specifications provided by the study statistician; have working knowledge of MS Office Suite and SigmaPlot. Knowledge of UNIX operating system and project management skills are preferred. A BA or BS degree in statistics or related fields is required, a MA or MS in these fields is preferred.

The Job Identification Number for this position is: 00-0001753uf

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