SAS Programmer I

1 mese fa


Milano, Lombardia, Italia PSI A tempo pieno

Job Description

You will contribute to statistical programming activities related to global clinical trials, working closely with international teams of statisticians, programmers, and data managers. Your tasks will include programming data sets and summaries.

Your Responsibilities

  • 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
  • Prepare and review program documentation
  • Produce TFL
  • Communicate with project teams and company departments regarding statistical programming of clinical research projects

Qualifications

  • University and master's degree in applied science, mathematics, statistics, or a related field
  • Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience working in the SAS system
  • Good knowledge of programming logic, SQL, and macro programming is preferred
  • Intermediate English, spoken and written
  • Experience within clinical trials and/or biostatistics
  • Good analytical skills
  • Proficiency in standard MS Office applications
  • Excellent communication and interpersonal skills

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