Position: Contract SAS Programmer (Full Time & Up to 3 days home working)
Start Date: Feb/Mar 2013
Location: UK (Commutable from London)
Rate: Competitive

Role

I am currently working on an opportunity for an experienced SAS programmer to join a top 15 pharmaceutical company as a clinical SAS programmer. The role would require someone who has an excellent and up to date SAS knowledge with experience using SAS in a clinical trials environment. Experience within clinical trials and drug/compound development is essential for this role.
The role will include responsibilities in data manipulation, analysis and reporting on clinical trails. Experience in working to CDISC standards will be beneficial. Working on dataset creation tables, figures, listings and graphs will be a key responsibility. Other responsibilities include program validation/documentation, output verification and QC of work done.
 

Requirements

• Excellent understanding of drug development (Pre-clinical Development, Clinical Development, Medical Affairs).
• Good knowledge of clinical trials within Pharmaceutical/Biotechnology/Medical environment.
• Excellent statistical analysis background/experience.
• Excellent understanding of statistical programming languages including SAS.
• Clear and effective communication of statistical information (written and oral)

• BSc or higher degree in a Statistics, Biostatistics, Mathematics or other subject with high statistical content.

Recruiting experts in Life Sciences

HAYS  Recruiting experts worldwide
 
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