CK Clinical, the leading independent pharmaceutical recruitment consultancy are recruiting for a Statistical Programmer for a leading CRO based in Wales.
This Statistical Programmer role will involve taking responsibility for the statistical analysis and reporting of a number of phase I clinical trials, providing input into clinical study protocols, writing statistical analysis plans, performing statistical analyses and reporting of TFLs to internal management and to external clients.
The main responsibilities of this Statistical Programmer role will include:
- Providing statistical input into the planning and development of clinical study protocols by creating/adapting the appropriate statistical requirements.
- Being involved in the creation of statistical analysis plans including the designing of data listings, table and figure shells for external clients in liaison with project managers.
- Providing clinical SAS programming support to projects according to specifications within the statistical analysis plan.
We are interested in applicants that hold an MSc in Statistics with proven experience as a Statistician working for either a Pharmaceutical/CRO/Biotechnology organisation. The ideal candidate for this Statistical Programmer role will also have substantial SAS programming expertise in the BASE, STAT and GRAPH modules of SAS (v9.1.3) to create listings, tables and figures. Working within Phases I & II is also desirable.
For more information, or to apply for this Statistical Programmer online now, please contact Priya at CK Clinical on +44 (0) 1438 870028 or email an updated copy of your CV to: email@example.com.