Description
Clinical Information Standards Specialist 11- Month Contract Global Pharma Company based - South East - UK
Daily Rate - £Open
Start Date - January 2012
I am seeking a Clinical Information Standards Specialist to join a leading pharmaceutical company based in the South of England on an 11 Month Interim basis.
Main Responsibilities:
* Development, deployment, management and governance of clinical information standards needed to support drug development processes
* Acts as Clinical Information Standards (CIS) project manager for selected standards
* Create, govern and maintain CIS developed standards models
Requirements:
* Extensive experience in Data Management or other Clinical Research related fields
* Experience with CDISC standards including SDTM, and CDASH
Please contact me for further information or email your CV.