上海切尔西医药科技咨询有限公司招聘合同制临床研究协调员

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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：

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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