The ideal candidate shall provide statistical programming expertise
(preferably in SAS) in the production of analyses, tabulations, graphics,
and listings from clinical trial data. Key responsibilities and skills
include, but are not limited to, the following: Contribute to the
preparation of analysis plans. Prepare, document and test required
programs and procedure data displays in an efficient manner for inclusion
in integrated clinical. statistical reports and other similar reports.
Contribute to the integrated clinical/statistical report and other similar
documents. Ensure analysis data and programming code meet regulatory and
company standards and are consistently structured to permit efficient
programming and reporting. Perform quality assurance procedures on work
performed by others. Develop, test, validate, document, maintain and
execute software and/or systems using the currently endorsed tools or
support of production activities. Assist in the integration of data from
remote entry sites
Natalie Fforde
Curtis House
34 Third Ave
Hove
BN3 2PD
Tel: 01273 722366
Fax: 01273 325350
Mobile: 07769 700 222
Email: [log in to unmask]
www.fforde-management.com
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