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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.
* 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
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