Employer: :India Novartis Healthcare Private Limited
Location:Hyderabad
Description:Provide timely and professional ongoing management of project & clinical trial data, Phases I to III, by identifying and resolving errors and inconsistencies in CRF data and by maintaining the CDM Study Workbook to ensure consistently high standard database(s) with respect to cost, quality and timelines. Coordinate serious adverse event reconciliation and monitor listing review with the clinical teams, perform external data reconciliation (e.g. lab data) in order that databases can be declared clean and locked according to strict quality standards. In addition represent CDM in clinical teams, define trial level data management strategy and manage clinical trials.
Deadline: Saturday, January 8, 2011
Link: http://www.novartis.com/careers/index.shtml
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