Àü¹ÝÀûÀÎ CRA ¾÷¹«Study Preparation(Feasibility, Pre-study visit, IRB submission, etc) Site Management(Site Initiation, Monitoring, Close out visit)SAE handlingDocument ManagementPharmacy management•Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. •Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required. •Depending on your level of experience, you may assist in training and mentoring less experienced CRA¡¯s and/or manage CRA¡¯s working on international projects.
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