[广州]上海切尔西医药科技咨询有限公司

职位：合同制临床研究协调员
发布时间：2012-03-05
工作地点：广州
信息来源：中山大学
职位类型：兼职
职位描述
上海切尔西医药科技咨询有限公司 —— 合同制临床研究协调员-GZ （兼职）

招聘专业： 不限 招聘对象： 实习生

学历要求： 本科及以上 工作地区： 广州医院

招聘人数： 1 投递方式： hr@

联系人： 联系方式：

添加时间： 2012-3-5 截止时间： 2012-7-31

浏览次数： 1

岗位要求：

岗位要求： 工作时间：3天（工作日）8:00~17:00 2012年3月~2012年9月- Bachelor or above Degree in Medicine or Nursing is a MUST; - Familiar with hospital environment; - Excellent communication skills with doctors and patients; - Detailed orientated;- Organizational skills;- Ability to multi-task;- Can work under pressure; - Doctor or nurse who is interested in clinical research is preferred.有兴趣的同学可以将CV投至:hr@

详细描述： - To assist the site investigator to deliver high quality patient data in accordance with ICH/SFDA-GCP and as required by the SOPs and study protocol; - To participate in the recruitment and screening of research patients; - To be responsible for use of computer applications and other technology to enhance the efficiency of the workflow in study activities including data collection and query resolution; - To collect, prepare and submit of regulatory documents as per required by the site EC; - To attend site initiation meeting; - To prepare the documents for study monitor site visits; - To assist investigator in obtaining proper written consent from each study participant according to the requirement; - To perform functions necessary for completion of protocols including scheduling, patient enrollment, medical histories, clinical assessments, laboratory-phlebotomy and processing, diagnostic studies, dispensing of investigational medication and overall organization and logistics of study visits; - To complete and correct case report forms ensuring accuracy of all records connected with each research patients; - To assist the investigator to report and record all adverse events according to GCP Guidelines and the request of sponsor; - To maintain accurate record of all study supplies including lab kits, medications and other items dispensed to patients; - To maintain close contact with sponsor concerning patient enrollment, scheduling, dosing/dispensing, abnormal laboratory values and adverse events; - To ensure a smooth communication through the studies between the site investigator and Project team. Provide weekly timesheet to sponsor project team members; - To update the TMFs and ensure the accuracy and completeness of TMFs; - To perform other duties as required.

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