You will contribute to statistical programming activities related to integral 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
📌 SAS Programmer I (Ciudad de México)
🏢 Psi Cro
📍 Ciudad de México
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