Dear Allstat,

Please find below our latest contract vacancy based in the North of England.

If this role is of interest to you please send an updated CV to
[log in to unmask] or you can reach me on +44 (0)207 922 7126

This is a 6 month contract initially, looking to pay excellent rates
depending on experience.

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.

Educational Qualifications

Preferably degree or equivalent in science, mathematical or computer based
subject.
Some level of biology is a distinct advantage.

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.


Skills in the use of the following are preferred:
Microsoft Windows, NT server environment and SAS 8.1 or above on Windows.
Validation and Quality Processes
Knowledge of Good Clinical Practice, ICH and related validation and
documentation practices is required. Understanding of FDA and similar
regulatory submission requirements is also an advantage.

Project Team Skills
Ability to work as part of a large team including Programmers,
Statisticians, Medical and Data Management members. Ability to contribute
to project planning and specification development related to the SAS
programming activities.

Personal Competencies
Good communication, time management, and team working skills are essential.
A very thorough and analytical thinking approach is also essential.

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

--
View this message in context: http://www.nabble.com/JOB%3A-Hays-Pharma---Contract-SAS-Programmer---6-Months---North-England-tp20538179p20538179.html
Sent from the AllStat mailing list archive at Nabble.com.