Dear Allstat,
Please find below details of our latest opportunity.
This is a permanent role, office based in the UK - South East
The ideal 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)
For further details, please contact me directly at [log in to unmask]
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