Description
Key responsibilities:- Inputting into study designs, reviewing study protocols, conducting sample size justifications and writing statistical analysis plans and specification of tables, figures and listings shells.
- Production of tables, listings and figures and report writing.
- Develop, test and run SAS programs for the statistical analysis and reporting of clinical study data.
- Liaising with the Statistical Programmers in the reporting of clinical study data.
- Business development involvement through contribution to proposals and presentations to customers
- Provide support in driving system and process improvements, and to develop and implement solutions to improve the efficiency and quality of clinical study data processing and reporting.
Requirements:
- Degree level in statistics or another subject with a strong statistical component.
- Consultancy skills gained across a broad range of applications and proficiency with SAS are essential for this position.
If you are interested in hearing about 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 .