招聘人数：若干
到岗时间：不限
年龄要求：不限
婚况要求：婚姻状况
1.Assist clinical research team on data receiving, transferring and recording. 协助临床研究段对收集传输记录数据
2.Participate in all clinical document management 参与所有临床研究文档的管理（随访登记表，每家中心的30天，1月，6月，一年，两年，三年，四年，五年的文档管理，随访时间表，不良事件表，筛选入选表，实验室正常值范围表，检查报告的统计表，研究者联系方式表随时更新，和医院的交接表，档案夹(一家中心一份) ）
3.Prepare and conduct the investigator meetings including all the logistic, agenda and all clinical study related document.
4.Prepare documentation for Ethics Committee submission.
5.Coordinate receipt and distribution of clinical trial supplies.
6.Perform Source Data Verification to ensure accurate data is recorded.
7.Ensure all Serious Adverse Cardiac Events are reported and followed up.
Bachelor degree or above in Medicine or related field.
Proficiency in Microsoft Word and Excel and familiarity with use of database.
Basic knowledge of clinical trial methodology is preferred.
Result oriented.
Customer focus and teamwork.
Good communication skill, self-learning skill.
Proficient English & Chinese in both verbal and written.
Regional travel is required.
求职提醒：求职过程请勿缴纳费用，谨防诈骗！若信息不实请举报。
