Covance Jobshttp://jobsearch.covance.com Hong Kong jobs with Covance(c) 2009, Covance10Tue, 28 Jun 2016 05:29:52 EST1333244Assoc Project Mgr Study StartupC. Essential Job Duties: - Lead core project team during study start up phase and facilitate team's ability to lead extended/complete project team. Depending on size and scope of project, this job duty may be performed in collaboration with a Senior Project Manager and/or Project Director. - Ensure effective cross-functional teamwork among project team members including both internal and externhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333244Mon, 27 Jun 2016 13:10:47 GMT1326674Assoc Proj Mgr Study Startup- Lead core project team during study start up phase and facilitate team's ability to lead extended/complete project team. Depending on size and scope of project, this job duty may be performed in collaboration with a Senior Project Manager and/or Project Director. - Ensure effective cross-functional teamwork among project team members including both internal and external ancillary services. - http://jobsearch.covance.com/CustomJobDetail.aspx?id=1326674Tue, 21 Jun 2016 13:22:35 GMT1326094Clinical Research Associate IIWe are always looking for talented clinical research professionals for Clinical Research Associate positions (CRA) in Hong Kong. If you are already working in the clinical trial industry in site monitoring and study site management, we want to talk to you about your career development. Covance is committed to providing a clinical research career with purpose in a culture that values achievement. http://jobsearch.covance.com/CustomJobDetail.aspx?id=1326094Mon, 20 Jun 2016 05:33:59 GMT1324722Director Regulatory Submissions Asia Pacific- Manage the activities necessary to formulate/implement submission strategies. Also, manage the interactions and activities necessary for the maintenance of Clinical Trial Applications and Marketing Applications. - Responsible for ensuring regional staff are properly preparing submissions (content and format) to Regulatory Authorities and performing liaison activities related to specific projechttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1324722Wed, 15 Jun 2016 05:31:44 GMT1322661Clinical Research Associate IIRefer to Covance JD which includes: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaise with vendors and other duties, as assigned Responsible for all aspects of site management as prescribed in the project plans General On-Site Monitoring Responsibilities Phttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1322661Tue, 07 Jun 2016 05:17:33 GMT1321142Clinical Research Associate IIWe are always looking for talented clinical research professionals for Clinical Research Associate positions (CRA) in Hong Kong. If you are already working in the clinical trial industry in site monitoring and study site management, we want to talk to you about your career development. Covance is committed to providing a clinical research career with purpose in a culture that values achievement. http://jobsearch.covance.com/CustomJobDetail.aspx?id=1321142Tue, 31 May 2016 12:51:25 GMT1312921Project Manager Study Startup- Lead core project team during study start up phase and facilitate team's ability to lead extended/complete project team. Depending on size and scope of project, this job duty may be performed in collaboration with a Senior Project Manager and/or Project Director. - Ensure effective cross-functional teamwork among project team members including both internal and external ancillary services. - http://jobsearch.covance.com/CustomJobDetail.aspx?id=1312921Fri, 06 May 2016 06:06:03 GMT1308674Clinical Project Admin I*To support Clinical operation manager in Financial aspect of clinical trials * Assist with the management of study supplies and organize of shipments. * Create, update, track and maintain study specific trial management files, tools and systems * Track and follow-up on serious adverse events as assigned * Responsible for all aspects of study site monitoring visits, maintenance of study files, liahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1308674Mon, 25 Apr 2016 12:36:18 GMT1307761PM TrainerPlan, coordinate and facilitate training for functional teams for the following training features: on-boarding, continuing education and/or special project needs. Partner with functional team and/or design team to update and/or create new/existing training materials and formal/informal documentation related to training features mentioned previously. Collaborate with functional team on specified prhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1307761Thu, 21 Apr 2016 13:08:56 GMT