Junior SAS programmers
My client is one of the top 10 pharma companies andare looking for junior SAS programmers.
* The primary role is, as a member of a drug project team, to assist the drug Global/Regional Programming Leader to deliver high quality SAS databases, tables, listings and graphical reports to the project team.
* This output is used to support regulatory submissions, publications and commercial activities.
* You will be responsible for the quality of your own work and will be expected to manage tyour own daily planning.
* The job involves close project working with all members of a team particularly Statisticians for whom the programmer develops the analysis databases.
* The programmers also take an active part in protocol and CRF review. They are also responsible for the specification of the tables and listings template shells and the analysis data sets. All programming work is performed to Alderley Park developed GCP documentation standards.
Skills Required
SAS Programming:
* Base: Particularly basic data step manipulation, SAS dataset creation, variable derivation and use of base procedures etc.
* Reporting: Tabulate, Print, Report, Graph procedures
* Statistics: Good skills with basic statistical summaries like Summary, Freq etc. Some skills with more formal statistical procedures such as GLM would be useful but is not essential.
* Macro: Basic use of macro preferred but advanced use is not essential.
* Computer Platforms and Operating EnvironmentsSkills in the use of the following are preferred:
* Microsoft Windows, NT server environment and SAS 8.1 or above on Windows.
Desirable Experience
Pharmaceutical and Clinical Trials
* Two years or more of SAS programming in the clinical trial environment.
* Experience with different therapeutic areas and trial phases.
* Experience of working as part of a clinical project study team.
SAS Programming
* Development of SAS programs that create SAS analysis data sets from raw database files for use in further formal statistical analysis and general clinical trial or high level document reports.
* Development of SAS programs that create output tabulations, listings and figures used in clinical trial, high level documents, or publication reports.
* Working as part of a programming team within drug project areas.
Is this role is of interest to you please send your CV to [log in to unmask] or contact me at :
Kien-Sen Lee
Resourcer ~ Biostatistics Division
James Harvard Pharmaceutical Ltd
T. 020 7922 7126 F. 020 7922 7101
Kien-Sen Lee
Resourcer ~ Biostatistics Division
James Harvard Pharmaceutical Ltd
T. 020 7922 7126 F. 020 7922 7101
E: [log in to unmask]
W: www.jamesharvardpharma.com
25 - 27 Wootton Street : Waterloo : London : SE1 8TG
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