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
- 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.
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