Description
Your Main Activities:* Proficient in SAS
* Knowledge of the programming and reporting process
* Knowledge of Guidlesines/System Life Cycel methodoolgie, ICH-GCP and any other applicable local and international regulations such as 21 CFR 11 and proven practical application.
* Develop, test and run SAS programs for the statistical analysis and reporting of clinical study data. This includes programs for derived datasets, CDISC (SDTM and ADaM) datasets, tables, figures and listings and their validation.
* Provide project support to the statistics reporting process through the specification of tables, figures and listings shells, writing of derived dataset specifications and the formatting of report documents and tabulations.
* Validate software, in the role of system tester, and test SAS Macros, maintaining the required validation and testing documentation
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Your Essential Skills:
-5+ years of relevant Statistical Programming experience.
-Working knowledge of population statistics and analytic techniques
-Experience within an epidemiological, health economics or outcomes research group
-Demonstrable record of collaborative working
-Experience in working with large observational healthcare datasets
-Experience in the pharmaceutical industry
If you are interested in this role, have any questions about this position or would like to register your interest in other positions, please feel free to send your up to date CV or contact me on