SAS Programmer

Essential, 5 years SAS programming experience (up to v8.2), 3 years recent pharmaceutical / CRO experience, SAS/base, SAS/macro, SAS/stat, SAS/graph and minimum of 1 year full study OR study reporting. Working with this massive international pharmaceutical company you will be providing SAS programming support for the analysis and reporting of clinical trials data. Your duties will include; review of database design specifications, export data from eCRF database / if applicable perform conversion to data sets, review database following eCRF data clean / highlight all data issues to study Data Manager, write / validate SAS programs for the production of output for data visualistions / key biometric result / full study reports, perform independant QC of SAS programs / outputs, ensure documentation of programming tasks is complete & assist with statistical programming process development.

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