Covance Jobshttp://jobsearch.covance.com Regional, PR jobs with Covance(c) 2009, Covance10Thu, 23 Oct 2014 05:19:59 EST1047695Sr Clinical Research AssociateJob Duties: - 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: o Ensure the shttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1047695Sat, 18 Oct 2014 11:22:32 GMT1047507CRAssistCovance is growing our CoSource team in Puerto Rico - Conducts site monitoring of clinical research studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP - Provide clinical support for projects according to Covance Standard Operating Procedures, ICH Guidelines and GCP - Site management responsibility for clinical studies according to Covance Standard Operating Prochttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1047507Sat, 18 Oct 2014 11:21:23 GMT1047278Clinical Research AssociateLocation : Portugal - home-based (ideally Lisbon region) You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Covance is one of the world's most exciting and professional drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries. We are looking for Clinical http://jobsearch.covance.com/CustomJobDetail.aspx?id=1047278Sat, 18 Oct 2014 11:20:19 GMT