職位描述
崗位描述：
1. 協(xié)助主要研究者進(jìn)行臨床試驗(yàn)的組織、實(shí)施，包括倫理申報(bào)，受試者篩選，受試者合格性判斷，參與試驗(yàn)程序，完成病例報(bào)告表等工作；
2. 協(xié)助主要研究者進(jìn)行醫(yī)療觀察和不良事件的監(jiān)測(cè)與處置，做好各項(xiàng)醫(yī)療工作，保障受試者的安全和試驗(yàn)項(xiàng)目的順利進(jìn)行；
3. 學(xué)習(xí)和參與試驗(yàn)方案的討論，參與方案的制定；
4. 負(fù)責(zé)臨床研究文件的準(zhǔn)備、收集記錄和管理；
5. 與主要研究者、申辦方、監(jiān)察員及倫理委員會(huì)溝通協(xié)調(diào)項(xiàng)目相關(guān)工作。
任職要求：
1. 有醫(yī)師資格證書，醫(yī)學(xué)本科及以上學(xué)歷；
2. 工作態(tài)度嚴(yán)謹(jǐn)，責(zé)任心強(qiáng)，有良好的溝通、協(xié)調(diào)能力，具備團(tuán)隊(duì)合作精神；
3. 有臨床試驗(yàn)相關(guān)工作經(jīng)驗(yàn)者優(yōu)先；
4. 中英文溝通能力佳者優(yōu)先
工作地點(diǎn):
天津經(jīng)濟(jì)技術(shù)開發(fā)區(qū)
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
