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Ref: 0512/11a

CONTRACT: SAS Programmer
Based in South East, UK
£ Excellent Rate / hour - 6 month rolling


For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to [log in to unmask]

Job Summary:

1.      At least 5 years of SAS programming experience in pharmaceutical and/or CRO environment
2.      Very good SAS programming knowledge (Base SAS, SAS/GRAPH, SAS/STAT, macro programming, reporting, SQL), familiarity with ODS RTF/ HTML
3.      A sound understanding of basic statistical principles and the basics of statistical programming
4.      Knowledge of the data management process in clinical drug development
5.      Good knowledge of medical coding processes, standards and issues
6.      Expertise in working with pooled, safety and efficacy data
7.      Good analytical skills
8.      Excellent interpersonal and team working skills
9.      Good communication and presentation skills, both oral and written
10.     Knowledge of regulatory requirements, e.g. ICH guidelines for statistical reporting
11.     Comprehensive knowledge of clinical and pharmaceutical drug development process and GCP requirements
12.     Multiple phase experience in clinical research
13.     The ability to work independently and prioritise your own workload

Highly Desirable:

Experience in safety data analysis
Programming skills in any of the following: JavaScript/VBScript, Java, VBA, XML, XSLT, SQL, Microsoft Excel
Exposure to investigational new drug application (IND) annual reports and Development Safety Update Reports (DSURs)
Experience of signal detection in clinical data

For further details or a confidential conversation please contact me directly:


James Carrera
Pharmaceutical Division
Statistics, Biostatistics & Programming
Tel: +44 (0) 207 255 6665
[log in to unmask]
http://uk.linkedin.com/in/jamescarrera

Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician

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