SAS Programmer I

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

Requirements

• 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
• 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

Please submit your CV in English.