Dear Allstat,
Please find below the details for our latest contract position based in the
South East.
If this position is of interest to you please send an updated CV with rate
expectations to [log in to unmask] or alternatively call me +44
(0)207 922 7126
My client has recently been given the go ahead to recruit an additional
Contract SAS Programmer to join their team in the South East to work full
time in their offices.
This is a 6 month contract initially with the opportunity to extend beyond.
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 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 and Trial Statistician 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
--
View this message in context: http://www.nabble.com/Job%3A-Hays-Pharma---Contract-SAS-Programmer---South-East-UK---6-months-initially-tp20362640p20362640.html
Sent from the AllStat mailing list archive at Nabble.com.
|