Dear Allstat,
Please find below details of our latest opportunity.
SENIOR SAS PROGRAMMER - The role is full-time permanent employment - UK South East - Office based
The candidate will be responsible for producing and validating statistical analysis using SAS. The Senior SAS Programmer has the overall responsibility of the reliability of output produced within a project and is in charge of training and supporting Statisticians and SAS Programmers on programming subjects.
Principal accountabilities include:
• Development and validation of SAS programs for the statistical analysis of study data finalized to the preparation of tables, listings and figures.
• Creation of randomization lists.
• Programming and validation of analysis datasets.
• Development of SAS programs for the management of clinical study data (i.e. datasets mapping, pooling, import/export, etc.).
• Preparation of trainings on programming subjects.
• To provide guidance to the programming biostatistics team on all data procedures and technical standards.
• To provide a work direction on all programming tasks within a project.
Profile:
The ideal candidate will have:
• At least 5 years of experience in statistical programming field or similar in a pharmaceutical environment or equivalent
• Bachelor degree in Statistics or related field preferred
• Good knowledge of CDISC standard. SDTM in particular
• Good knowledge of descriptive and inferential statistics and statistics modelling
• Good knowledge of pharmaceutical industry guidelines like ICH, GCP etc
• Good English (both written and spoken)
If you are interested in further details, please contact me directly at [log in to unmask]
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