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Clinical SAS Programmer Wilmington United States,  

Posted on : 23 May 2017

Project Description

  Under the supervision of a Sr. Clinical Database Programmer and the Manager, Clinical Database Programming, the Database Programmer is responsible for producing standard and custom reports for use by the Clinical Data Managers in their data review and cleaning efforts, developing transfer specifications with vendors for external data sources, performing Study Data Tabulation Model (SDTM) conversion programming and Quality Control (QC) and handling all other ad-hoc data requests by project team members for assigned studies.   Job Responsibilities:   Extract clinical data from the clinical data management system and produce standard and custom reports, primarily in SAS  Program reports and listings as requested by project team members for ongoing studies  Develop transfer specifications with vendors for external data sources  Perform consistency checks on data transferred between Incyte and external parties to ensure completeness and accuracy of data contained transfers  Perform programming to convert raw, clinical trial data to Study Data Tabulation Model (SDTM) format  Perform Quality Control (QC) on programming work performed by fellow Database Programmers  Create and validate global macros or systems that streamline repetitive operations to increase programming efficiency  Other duties, as assigned.    Minimum Requirements Bachelor?s degree OR certification  Minimum of 5 years of clinical SAS programming experience in the pharmaceutical industry  Working knowledge of CDISC SDTM  mapping/specs/conversion/domains/datasets/eCRF/eCRT Package/define.xml development and SDTM data transfer operations on clinical studies  Good understanding of regulatory requirements relevant to submissions  Good knowledge of clinical trial study design and electronic data submission requirements  Good communication and interpersonal skills and the ability to work effectively as part of a team    


Wilmington DE

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