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Senior Statistical Programmer, 12 months (South East, UK)

My client has just got the go ahead to recruit a Senior Statistical Programmer initially for 12 months to be based in the South East, UK. You will be working for a leading pharma client that is excellently located in the M4 corridor. Excellent Rates for the right candidate

Responsibilities and Duties include providing statistical programming and validation support for clinical study reports, overseeing programming activities by a CRO and coordinating programming activities among the study programmers to achieve timely progress in the following areas: analysis datasets, statistical tables, figures, listings, (ISS), (ISE), electronic submissions and other internal and external requests (e.g., publications). You will be working with a CRO to develop and monitor the content and structure of SAS data sets.

You will be required to have experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. Project management experience in a pharmaceutical/CRO programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical/CRO environment is required. This is an fantastic opportunity to work on a long term contract where there is an excellent chance of extending beyond the initial contract period.

For further information please don't to contact me immediately.

Mark O'Brien
Divisional Manager, Biostatistics - Hays Pharma
t. +44 (0) 20 7922 7106
mark.o'brien@HAYSPHARMA.COM

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