Dear Allstat,
A great opportunity to join one of the industries leading pharmaceutical
organisations and take on programming responsibilities for high profile
clinical projects.
Rates of pay are highly competitive, contract is long term and
extendable. Call Alan Brophy on 0207 255 66 00 for full details.
**We can consider candidates with non clinical/pharmaceutical SAS
experience for these assignments**
SAS Programmers perform an important role in the UK Programming Section
of our client, one of the industries largest pharmaceutical
organisations. Their primary role is to assist the Drug 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.
Programmers are responsible for the quality of your own work and are
expected to manage your own daily planning.
This role involves close project working with all members of a team
particularly Statisticians for whom the programmer develops the analysis
databases. The programmers will also take an active part in protocol and
CRF review. They are responsible for the specification of the tables and
listings template shells and the analysis data sets. All programming
work is performed to client developed GCP documentation standards.
Qualifications and Experience:
Preferably BSc degree or equivalent in science, mathematical or computer
based subject. Some level of Biology is a distinct advantage.
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.
Desirable Experience:
* 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.
* 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.
To apply forward your CV with a short cover note detailing rate
expectation and availability to start to [log in to unmask]
Alternatively call Alan Brophy on 0207 255 66 00 for further information
and confidential discussion of this opportunity.
Best regards,
Alan Brophy
SEC Recruitment, London
Tel: 00 44 (0)207 255 66 00
SEC are a Recruitment and Employment Confederation (REC) member and
ISO9001:2000 accredited specialist recruitment organisation working
within the Pharmaceutical, Biotech and CRO industries. If you are
interested to learn more about further appointments within Biostatistics
or Statistical Programming across the UK and Mainland Europe contact
Alan on 020 7 255 6600 for a confidential discussion.
SEC Recruitment Limited is acting as an Employment Agency and/or
Employment Business
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