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È«ÇòÊ®´óÒ©³§Ö®Ò»£¬¼±ÕÐ5ÃûMedical Reviewer£¬ÒªÇóÁÙ´²Ò½Ñ§±ÏÒµ£¬ÖÁÉÙÒ»ÄêÒ½Ôº¹¤×÷»òʵϰ¾Ñ飬»òÒ©³§¹¤×÷¾Ñé¡£Ó¦½ì±ÏÒµÉúÒ²¿ÉÒÔÉêÇëClinical Data Coordinatorְλ¡£ 1. Conduct medical validation/review tasks directly, or by coordinating the work of others. Coordinate related tasks taking into account directions from CSD through medical validation/review plan, other type of quality documents, or through direct communication. Ensure that activities are conducted in adherence with quality standard, and that deliverables are met, in accordance with CSD needs, and with respect to study timelines. 2. In collaboration with CSD and clinical scientist, and with their input, define clear goal and expectations for medical validation/review according to compound safety profile, study population characteristics, study design and efficacy criteria. 3. Communicate regularly on tasks advancement and completion, difficulties encountered, and potential delays. 4. Define timelines for completion of each task, in coordination with team leader, and CSD. 5. With team leader, and taking into account CSD perspective on the task allocated, allocate resources for the task and prioritize 6. Actively transversal communicate with other functions (eg TO, GPE, CSU, CDOC, TIM and so on) to resolve safety data issues timely and effectively ¸ÐÐËȤµÄÇë·¢¼òÀúÖÁstefanieli@chinacareer.com |
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