On behalf of our Client a global pharmaceutical company, IQVIA is looking for a Lead Statistical Programmer who can join an exciting working environment in a dynamic atmosphere.
- To develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD.
- To guarantee quality of statistical output produced by external provider, to program tools to support data review activities and data visualization, to collaborate on the interpretation and communication of trial results.
- To contribute to regulatory submissions, converting data according to regulatory requirements, preparing integrated analyses and related documentation.
- To perform post-hoc analysis for exploratory purposes, or to support regulatory requests, to prepare analysis for paper publications.
- To support the development of standard operating procedures
Long Term contract – Staff Leasing