Covance Jobshttp://jobsearch.covance.com Buenos Aires, ARG jobs with Covance(c) 2009, Covance10Fri, 24 Jun 2016 11:17:52 EST1326681Clinical Project AdministratorCovance is hiring a clinical project administrator in Buenos Aires! Essential Job Duties: - Provide clerical support to project team. - Provide telephone coverage and related support duties - Set up and maintain clinical investigator files and documentation - Prepare investigator budget payments and tracking systems, generate tracking reports as assigned. - Data entry and maintenance of selehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1326681Tue, 21 Jun 2016 13:24:41 GMT1323309Clinical Team LeadYour responsibilities in this position would include: Study Set up: - Organizes kick-off meeting with monitoring team (MTs) - Organizes training of monitoring teams (study procedures, study devices, monitoring plan, etc) - Organizes investigators meetings (local, cluster or regional) as applicable - Provides support to MTs (protocol, monitoring plan, CRF, tools etc.) - Arranges the preparatihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1323309Thu, 09 Jun 2016 05:26:30 GMT1320690Sr Clinical Research AssociateClinical Research Associates – CRAs are needed in Buenos Aires due to continued growth! Extreme need for oncology Experience . Una carrera gratificante Recibira una extra AR $43,500 en tu primer mes con nosotros! Responsibilities Include: - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of phttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1320690Fri, 27 May 2016 06:20:34 GMT1320402Sr Clinical Research AssociateEssential Job 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 visit; liaise with vendors; and other duties, as assigned. - Responsible for all aspects of site management as prescribed in the project plans - Ensure the study staff who will conduct the protohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1320402Thu, 26 May 2016 06:15:29 GMT1318820Clinical Research Associate I MEA- In this position candidates complete the Covance Monitoring Excellence Academy (MEA) training program - Provide clinical support for projects according to Covance Standard Operating Procedures, ICH Guidelines and GCP - Develop and/or maintain tracking systems for clinical projects - Assists teams and conducts site monitoring of clinical research studies according to Covance Standard Operatinhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1318820Fri, 20 May 2016 12:55:21 GMT1317624Clinical Research AssistantJob Duties: - Act as contact for project team and study sites - Perform CRF review, query generation and resolution against established data review guidelines, under direct supervision on Covance or client data management systems, as assigned by management - Assist with generation and reconciliation of queries to investigative sites/clients to resolve problem data - Assist with the management http://jobsearch.covance.com/CustomJobDetail.aspx?id=1317624Tue, 17 May 2016 12:57:07 GMT1314927Associate Global Site ServicesCovance is seeking new members for our site services team in Buenos Aires! As a Global Site Services Associate your responsibilities will include: Job Summary: - Primary contact with investigative sites during site start-up activities with responsibility for collection of the required investigator and regulatory documents for a study and ensuring that the documents meet the specifications requihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1314927Mon, 09 May 2016 12:48:25 GMT1301377Associate Global Site ServicesCovance is growing again in Buenos Aires, Argentina! Main Responsibilities: - Collect, review, process, and track regulatory & investigator documents required for study site activation in accordance with Covance SOPs, sponsor SOPs, ICH GCP guidelines, EU Clinical Trial Directive, FDA Regulations and the Investigator Package Plan. - Assist in review and approval of regulatory & investigator docuhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1301377Thu, 31 Mar 2016 12:51:38 GMT