[北京]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：2011-11-10
工作地点：北京
信息来源：中山大学
职位类型：全职
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-BJ

招聘专业： 临床，药学，护理 招聘对象： 应届生

学历要求： 本科及以上 工作地区： 北京

招聘人数： 1 投递方式： hr@

联系人： 联系方式： 021-61132848

添加时间： 2011-11-10 截止时间： 2011-12-31

浏览次数： 3

岗位要求： - Bachelor or above Degree in medicine, pharmacy science or nursing;
- More than 1 year clinical monitoring experience in global oncology studies according to SFDA/ICH GCP;
- Self-motivated, interested in the clinical research work;
- Excellent interpersonal skills, negotiation skills and presentation skills;
- Good communication skills with fluent verbal and written English and Chinese;
- Willing to work at sites and can travel frequently;
- Teamwork spirit;
- Can work under pressure.

- 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 ofinvestigational 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 topatients; - 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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