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SAS Programmer II
Ref No.: 18-12534
Location: Bridgewater, New Jersey
Title - SAS Programmer II
Location - Bridgewater NJ
Duration - 04+ Months
​Only for W2



Provide statistical programming expertise (in SAS) in the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis data specifications. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical, statistical reports and other similar reports. Contribute to the integrated clinical/statistical report and other similar documents. Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting. Perform quality assurance procedures on work performed by others. Develop, test, validate, document, maintain and execute software and/or systems using the currently endorsed tools or support of production activities. Assist in the integration of data from remote entry sites, contract organizations and co-licensing partners to the central database.

Excellent technical skills in statistical programming, with advanced knowledge in SAS, and other statistical computing software.
Knowledge on regulatory requirement evolution (SDTM, SDRG, ADRG, ADAM, XML format, etc…); thorough understanding of pharmaceutical clinical development (i.e. understanding of statistical concepts, techniques and clinical trial principles).
Experience working on ISS/Client and related submission deliverables.
Ability to work independently and contribute with minimal supervision.