职位描述
岗位描述：
1. 协助主要研究者进行临床试验的组织、实施，包括伦理申报，受试者筛选，受试者合格性判断，参与试验程序，完成病例报告表等工作；
2. 协助主要研究者进行医疗观察和不良事件的监测与处置，做好各项医疗工作，保障受试者的安全和试验项目的顺利进行；
3. 学习和参与试验方案的讨论，参与方案的制定；
4. 负责临床研究文件的准备、收集记录和管理；
5. 与主要研究者、申办方、监察员及伦理委员会沟通协调项目相关工作。
任职要求：
1. 有医师资格证书，医学本科及以上学历；
2. 工作态度严谨，责任心强，有良好的沟通、协调能力，具备团队合作精神；
3. 有临床试验相关工作经验者优先；
4. 中英文沟通能力佳者优先
工作地点:
天津经济技术开发区
Phase I Clinical Research Physician
Job Description:
1.To assist principal investigator (PI) in charge of the clinical trials, including institutional review board (IRB) application, subject screening, verify subject eligibility, and other study procedures, complete case report form (CRF), etc.;
2.To assist PI for medical observation, adverse events (AE) recording, handling and reporting; responsible for physical examination; pay attention to the safety of subjects, ensure to complete the study conduct successfully.
3.To learn and participation in the protocol drafting and discussion.
4.To be responsible for the study sources preparation, collection and management;
5.To communicate with PI, sponsor, auditor and IRB.
Job Requirement:
1.Physician qualification certificate, Bachelor degree or above;
2.A good team player and can be motivated to conduct multiple studies.
3.Good communication skills both in English and Chinese.
4.Clinical trial work experience preferred
Job Location:
Tianjin TEDA
