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ALLSTAT  July 2011

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Subject:

Re: SAS Programmers Required for September

From:

Russell Gillam <[log in to unmask]>

Reply-To:

Russell Gillam <[log in to unmask]>

Date:

Fri, 29 Jul 2011 17:37:30 +0100

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (59 lines)

**** SAS Programmers****

Contract SAS Programmers required:

-12 Months Contracts - Pharmaceuticals
Surrey, UK
40 - 45 p/h


-6 Months Contract - Pharmaceuticals
West Germany
70 - 80 EURO P/H


SAS PROGRAMMER:

Your Accountabilities/Responsibilities:
Provide advanced level of SAS programming activities for the monitoring
Collaborate with project biostatistician in the creation, implementation, and maintenance of execution plan accounting for timeline, resource and quality of the projects
- Ensures that all statistical programs comply with the programming coding standards and utilize available standard reporting systems, as well as macro utility programs.
- Support statistical programming applications that are used to generate clinical study reports.
- Support ADS and TLG generation, and assist with the development of work flow and SOPs for Biostatistics and Statistical Programming operations.
- Accountable for the provision of standard and non-standard data sets, tables, listings and figures based on the final synopsis and SAP that are required for the study reports, submissions and product defense.
- Communicates effectively not only within the teams and functional lines but also with the external resources
- Provides filing, approval and regulatory programming support for all aspects of a submission

Your Qualifications:
Degree in life sciences, statistics, biostatistics, or equivalent areas with extensive experience in pharmaceutical industry, medicine or a relevant field is preferred.
Extensive SAS programming skills
Knowledge of base SAS, SAS macro language, graph, FSP, STATS, SQL as well as other programming languages.
- Knowledge of Unix system, Oracle Clinical and EDC (electronic data capture) exposure preferred excellent analytical, problem solving, and computer skills.
- Basic knowledge of FDA/ICH guidelines, the software development life cycle, and 21 CFR Part 11 and other FDA regulations.



If  you would like a confidential discussion in regards to this exciting opportunity, then please feel free to get in touch on +44 207 255 6665 OR alternatively send your updated CV to [log in to unmask]<mailto:[log in to unmask]>












________________________________
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