[武汉]上海切尔西医药科技咨询有限公司

职位：临床研究协调员
发布时间：2015-10-21
工作地点：武汉
信息来源：武汉大学研究生就业网
职位类型：兼职
职位描述
单位性质：其他企业

单位行业：医药/生物工程

单位规模：50人-100人

单位所在地：上海市 上海市徐汇区 漕溪北路398号汇智大厦502
职位信息

职位名称： 临床研究协调员-武汉 招聘人数：1

发布时间：2015-10-21 截止时间：2017-10-31

招聘对象：实习实训 学历要求：本科及以上

工作地点：湖北省武汉市硚口区

专业要求

博士：临床医学

硕士：中药学，制药工程，护理学，药理学

本科：临床医学，护理学
职位描述

Clinical Research Coordinator (CRC,临床研究协调员)

工作地点：武汉市三甲医院

工作时间：每周2个工作日

Responsibility:
- 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.

Requirements:
- 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 has digestive experience and is interested in clinical research is preferred.

感兴趣的同学也可将简历以附件形式发送至hr@。优先考虑2014年入学研究生/研二学生

企业简介ENTERPRISE INTRODUCTION
Chelsea Clinical Research is a Shanghai-based Contract Research Organization (CRO) which provides a comprehensive range of clinical trial services to international pharmaceutical companies, biotechnology companies and research institutions in China.

Our mission is to deliver service excellence and timely, quality results for our clients. As a professional drug development organization, we believe in the value of building trusted partnership with our clients.