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If interested please contact Kien-Sen Lee at 
[log in to unmask] or on +44 (0)207 9227126.  Please do not 
reply to this email address.



Dear Allstat,

Please find below the details of our latest Contract SAS Programming
opportunity.
Rates are dependent on experience and there is plenty of scope to
extend.

My client is one of the top 10 pharma companies and are looking for 2 x
Contract 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 your 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.

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 Environments
Skills 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
Experience 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.

If this position is of interest to you please forward an updated CV to
[log in to unmask] or alternatively for a private consultation
call me on 00442079227126

Ian Kien-Sen Lee
Consultant, Biostatistics - Hays Pharma
t. +44 (0) 20 7922 7126  f. +44 (0) 20 7922 7101  m.+44 (0) 7957 952775

We will be exhibiting at the Phuse conference in Manchester, UK in
October. Please come and visit us at the Hays Stand.

LinkedIn Profile - http://www.linkedin.com/in/Kiensen

Hays Pharma is part of the Hays Plc group of companies - for all our
latest jobs and industry news go to www.hayspharma.com.

Please consider the environment before printing this e-mail
Hays Pharma is proud to be a Carbon Neutral Company
http://www.carbonneutral.com/


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Hays Pharma is a member of the Hays Plc group of companies. Hays Plc 
is registered in
England and Wales, number 2150950. Registered office, 250 Euston 
Road, London, England, NW1 2AF.
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James Miller
Department of Statistics
University of Glasgow
15 University Gardens
G12 8QQ
0141 3302474
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The University of Glasgow, charity number SC004401