Amgen
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
Please email resumes to tevarts@amgen.com and visit www.amgen.com for
more information about Amgen.
EEO/AA Employer M/F/D/V