Covance Jobshttp://jobsearch.covance.com Hong Kong jobs with Covance(c) 2009, Covance10Wed, 04 Mar 2015 10:59:20 EST1093257Senior Clinical Research Associate-Responsible for all aspects of study site visits and site management and monitoring activities ex. f/u SAE, clinical supply, etc -Prepare accurate and timely trip report -review progress of projects and initiate appropriate actions to achieve targets -feasibility work, site selection, EC submission, RA submission, translation of study documents, negotiate study budget, contract - Assist with traihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1093257Wed, 28 Jan 2015 13:01:27 GMT1091059Clinical Research Associate IIResponsible for study startup which include IRB/IEC submission, site selection, recruitment of potential investigators, notifications to regulatory authorities, translation of study-related documentation Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned Responsible for all aspects of study site monitoring includhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1091059Wed, 21 Jan 2015 13:01:42 GMT1082533Study Director ToxicologyDuties and Responsibilities: - Coordinates efforts of the study team. - Learns to review cost estimates to ensure that all protocol/amendment driven workscope specifications have been included in the price estimation. - Understands financial status of ongoing studies. - Learns to develop protocols and ensures that the protocol, including any changes, is approved, and is in compliance with apprhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1082533Tue, 30 Dec 2014 13:01:32 GMT