외국계 CRO사-Senior Clincial Research Associate
페이지 정보
등록자 :
강대필상무
등록일 : 14-11-10 00:00
기본정보
외국계 CRO사-Senior Clincial Research Associate | |||
임상 | 사원~과장 | ||
무관 | 무관 | ||
서류전형 -> 1차면접 -> 2차면접 | |||
상세정보
본문.Responsible to support project team(s) on all project-related issues to ensure all activities are conducted in highest quality standards, in compliance with ICH E6 GCP, local GCP and applicable local regulatory requirements as well as to meet/exceed sponsor''''s expectation, under the supervision of project manager(s) .Support to develop, compile and/or review all study-related regulatory and administrative documents from investigational sites, monitoring visit reports, work progression reports and other study-required documents .Support to develop, compile and/or submit dossiers to regulatory and/or ethics committee for review and follow up until approval, if required .Support in planning, coordinating, organizing and attending all study-related meetings and activities for sites as required
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