Senior SAS Programmer (19-00813) – NJ – paramus

Bachelor’s degree with 9 plus years Pharmaceutical/CRO experience as a SAS Programmer supporting clinical trials for regulatory submissions; or 8 plus years experience with a MS/MA degree. Responsibilities will include, but are not limited to, the following: • Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells. • Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs. • Perform ad hoc flexible and rapid programming arising from questions generated from planned analyses and results. • Ensure consistency and adherence to standards within their therapeutic area. • Provide input to the design of the clinical…

Source: Job Diva – Job Listing

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