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Responsibilities: - responsible for all implementation in SAS of any outputs of the clinical reports. - collaborate closely with the project programmer to implement template programs - participate in the blinded report planning meeting (BRPM). - together with the Trial Statistician, the TPROG is responsible for the Mock Report SAS implementation, including the analysis datasets, tables, graphs and listings and according to the TSAP specification Key requirements for the position: - a Trial programmer should have a very good SAS V9 experience with at least 3 years in Clinical report SAS implementation (Efficacy and Safety part) As a Trial SAS Programmer you will receive benefits like: - Professional training - Great salary package - Career development within a leading pharmaceutical company If you have the skills and experience for this opportunity please email your C.V. to [log in to unmask] or call +44(0)1273 727 930 for further details. Andrea is a Biometrics expert at Stelfox Pharmaceutical Search covering Europe, UK, North America and Asia. You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.