Dear Allstat,
Please find below details of our latest contract Statistical Programming
vacancy.
If this opportunity is of interest for you and would like to discuss it
further please send an updated CV to [log in to unmask] or contact me
on +44(0)207 7633 4824
Our Client, a World Leading Pharma, are looking to employ a two Senior SAS
Programmers with strong experience in Tables, Listings, Figures and Graphs
through phases I – IV to work in the UK. The contracts are initially 12
months with strong opportunity for extensions and offer full time home
working.
Contract SAS Programmer
Summary
To coordinate the programming aspects of assigned clinical trials and to
develop programs and tools for the management, reporting and analysis of
clinical trial data.
Main Responsibilities
Technical design, programming and QC of SAS programs for the management,
reporting, analysis and submission clinical trial data.
Accountable for ensuring compliance with ICH GCP, relevant SOPs and
guidelines and standards
Where assigned the Trial Programmer (TPROG) role for the study, take
responsibility for the programming tasks, including planning, the provision
of programs to assist in ensuring data quality and reporting of the data.
Be fully responsible for the quality of the analysis data, data displays and
derived submission data
The use of SAS to meet the business needs of Biometrics and Data Management
Ensure agreed timelines relating to reporting of data are achieved
Liaise with the Trial Data Manager (TDM) and Trial Statistician (TSTAT) as
required to ensure programming is effective in the support of data quality,
reporting and analysis across the trial
Support users in resolving programming issues or issues related to the use
of SAS
If this opportunity is of interest for you and would like to discuss it
further please send an updated CV to [log in to unmask] or contact me
on +44(0)207 7633 4824
Best regards
Ben Cowley
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