Job DescriptionPlease submit your CV in English.You willcontribute to statistical programming activities related to global clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets andsummaries.You will:Develop analysis data sets structureDevelop program requirements and specificationsBe involved in SAS programming of ADS and Tables, Listings and FiguresSupport SAS program validationsPrepareand review program documentationProduce TFLCommunicatewith project teams and company departments with regard to statistical programming of clinical research projectsQualificationsUniversity and Master's degree in Statistics or BiostatisticsKnowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS systemGood knowledge of programming logic, SQL and macro programming is preferredProficient inEnglish, spoken and writtenExperience within clinical trials and/or BiostatisticsGood analytical skillsProficiency in standard MS Office applicationsExcellent communication and interpersonal skillsAdditional InformationOur mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors.Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.
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