SAS Programmer I

2 giorni fa

Milano, Italia PSI CRO A tempo pieno

Job Description Please 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 structure Develop program requirements and specifications Be involved in SAS programming of ADS and Tables, Listings and Figures Support SAS program validations Prepareand review program documentation Produce TFL Communicatewith project teams and company departments with regard to statistical programming of clinical research projects Qualifications University and Master's degree in Statistics or Biostatistics Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system Good knowledge of programming logic, SQL and macro programming is preferred Proficient inEnglish, spoken and written Experience within clinical trials and/or Biostatistics Good analytical skills Proficiency in standard MS Office applications Excellent communication and interpersonal skills Additional Information Our 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. #J-18808-Ljbffr

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