Main Job Tasks and Responsibilities: * Supports statisticians in programming inferential analysis, Tables, Figures, Listings and randomization in SAS to ensure accordance with the Statistical Analysis Plan and study protocol and complying with the rules and guidelines for validated SAS programming. * Helps in organizing and conducting a quality control review of the tables, listings figures, and inferential analysis to ensure compliance with the protocol and SAP. * Prepares and archives of all datasets, computer programs and other material used in the preparation of the tables, listings, figures, inferential analyses for the integrated study report in order to have a complete and transparent documentation of the whole process * Develops and maintains SAS programs and SAS full-screen applications to support the data management group. * Contributes to the development of SAS programming and related SAS applications (including implementation of the quality system for SAS programming) guaranteeing the best quality services of the department. Work experience: * Proven relevant experience of successfully performing the role of Statistical Programmer, in the clinical research industry. * Demonstrated ability to perform assigned tasks independently and as part of a team. * Demonstrated ability to successfully manage multiple tasks and timelines. * Demonstrated ability to liaise professionally with team members. * Strong working knowledge of data structures (e.g., CDISC SDTM, ADaM), software development lifecycle and their implementation. * Strong working knowledge of the development and use of standard programs and macros. Skills: * Demonstrated knowledge of and experience in the application of CDISC data and standards, primarily the creation and use of SDTM and ADaM datasets. * Extensive knowledge of statistics, programming and/or clinical drug development process and advanced knowledge of SAS. * Base & Advanced SAS Certified Programmer.