SAS Programmer I.

hace 2 meses

Mexico City PSI A tiempo completo

Job Description

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

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

Qualifications

University and master's degree in applied science, mathematics, statistics or the like 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 in 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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