梦之岛
公司主要招聘CRA,职责及要求如下:工作职责:1.To perform clinical monitoring activities of designated projects in accordance with the APEX SOPs (or the Sponsor’s SOPs as appropriate), which include: investigator/site selection, managing and co-ordinating site related activities, collating regulatory documentation and IRB submissions, and monitoring activities (such as source data verification, drug accountability, etc.) throughout the study in accordance with the ICH GCP guidelines. 2.Also accountable for detecting, analyzing and solving technical, proceral and/or motivational problems that may occur to the site staff of the investigation team and thus affect the progress of the project. 3.Supporting local issues like SSU, project local issues; monitoring within the region. 职位要求:1.A bachelor (or above) degree in a life science (preferably paramedical) field. 2.More than 2 years’ work experience in clinical operations, particularly study monitoring. 3.Good communication skill and proactive attitude. 4.Ability to take initiative and work independently. 5.Ability to speak and read the language(s) used locally in the country, plus a fluency in written and spoken English. 6.Ability to travel – on both local and international trips. 详情请参考: http://www.yaojobs.com/Company/Company_Detail.aspx?ID=1753