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Position: Senior SAS Programmer
Duties: Participates in the validation of SAS programs and maintains validation documentation; Familiarizes oneself with the SAS dataset structure and format catalogue related to a given study; Familiarizes oneself with the documents associated with a given study. Such documents include (but are not limited to) edit check documents, SAS and database annotated Case Report Forms (CRFs), visit map/schedule of events, CRFs, code lists, statistical analysis plan (SAP), data management plan (DMP), clinical protocol, programming-specific documentation; Develops, programs and maintains
Requirements: Bachelor’s degree in the relevant field of study or B.S. equivalent; Minimum 5 years experience in clinical research required; Possess an intermediate level of understanding of data management practices and clinical data management systems (CDMS)
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