Stat Programmer Analyst II

Creates and maintains statistical analysis data sets incorporating data from multiple sources (internal and CRO). Programs or modifies existing programs to review data and generate tables, listings, and graphs. Assists in processing ad hoc requests. May oversee and coordinate work of other staff and CRO. 5 to 10 years relevant experience in biopharm industry with clinical trials work. Use of SAS in pharma environment and experience with clinical trials data. Experience with data structures and data management techniques necessary. Understanding of validation methodology and implementation required. SAS V8 experience highly preferred. Ability to comprehend study documentation (protocol, CRFs, other plans). Excellent understanding of data management principles. Detailed knowledge of basic statisitical concepts. Excellent understanding of base SAS, SAS macro language, SAS GRAPH, PROC SQL, and SAS Access. Excellent communication skills. BA BS in computer science, statistics, applied statistics, biology or related field. MA MS preferred.

The Job Identification Number for this position is: 00-0001755uf

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