Covance Jobs Buenos Aires, ARG jobs with Covance(c) 2009, Covance10Tue, 03 May 2016 04:42:12 EST1309395Clinical 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 sele, 27 Apr 2016 17:02:06 GMT1308755Clinical Research Associate ICovance is seeking an ENTRY LEVEL Clinical Research Associate to join our team in Buenos Aires! Job Duties: - Conducts site monitoring of clinical research studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP. - Provide clinical support for projects and site management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Gu, 25 Apr 2016 17:23:50 GMT1308754Associate Global Site ServicesCovance is seeking a site services associate to join us in Buenos Aires! 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 required by applicable regulations - Maintenance of allocated site's informatio, 25 Apr 2016 17:23:48 GMT1304936Specialist I Document Review MaintenanceDue to exciting growth, we are currently hiring a Document Review Specialist I in Latin America The Document Specialist will: - Liaise with operational project team regarding project issues (i.e., participate in team meetings) - Review and approve core Country patient informed consents for compliance to country requirements and protocol as applicable - Review and approve investigative site spe, 12 Apr 2016 12:15:35 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 docu, 31 Mar 2016 12:51:38 GMT1289631Sr Clinical Research AssociateCovance continues to grow in Buenos Aires We are seeking a Sr. Clinical Research Associate to join our team! - 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 manage, 03 Mar 2016 12:38:41 GMT1284234Sr Clinical Research Associate"For Recruiter Use Only" Job Description Education/Qualifications University/College degree (life science preferred). Experience Minimum four (4) years in clinical research monitoring Experience . EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confiden, 17 Feb 2016 06:30:19 GMT