A new permanent position has opened with one of our client based in France. They are looking for a SAS Programmer/Statistical programmer to join their team and act as a support for the biostatisticians and senior programmers. More detail available when you contact Louise Beka.
Your responsibilities will cover:
-Support senior SAS programmers and statisticians in maintaining efficient interfaces with internal and external customers.
-Program analysis datasets, pooled datasets, tables, figures and listings for phase I-IV clinical trials
-Ensure that documents and specifications are consistent and comply with company standards
-Provide input at meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities
-Keep records for all assigned projects including archiving of trial analysis and associated documentation
-Comply with pre-defined study standards and specifications
You will have the following profile:
-BSc/Msc in statistics, mathematics, computer sciences, life sciences, computer sciences or equivalent
-At least 4 years' experience as a SAS programmer in a pharmaceutical, CRO, Biotech environment
-SAS experience with SAS Base, SAS Graph, SAS Macro, and SAS Stat
-Fluent in English (spoken and written)
If you are interested in this position, please send your CV with a cover note by email at louise.beka@secpharma.com or for more details on the role or similar positions, please contact Louise Beka on +44 (0) 207 255 66 65