1. Assist Project Manager in project organization and execution,draft Project Management Plan(PMP) and Monitoring Plan(MP) under the guidance of Project Manager. 协助项目经理进行项目组织、实施,在项目经理指导下起草项目管理计划和监查计划。
2. Assist Project Manager in internal communication. 协助项目经理进行内部沟通;
3. Assist Project Manager in preparation and (or) submission of project documents such as ICF,Recruitment Advertisement and etc. 协助项目经理进项知情同意书、招募广告等项目文件的准备和(或)递交;
4. Responsible for project monitoring to ensure the quality of clinical operation. 承担项目监查工作,确保临床操作质量;
5. Assist the Project Manager in collecting and following up the project payments; 协助项目经理整理和跟踪项目款项;
6. Assist Project Manager in collecting and organizing clinical trial documents and completing documents handover with sponsor. 协助项目经理收集和整理临床试验文档,协助完成与申办方的资料交接;
7. Handle other matters arranged by the project manager.处理项目经理安排的其他事宜。
任职要求:
1. Clinical Medical,Pharmaceutical or Life Science or related background,with Bachelor Degree or above. 临床医学,药学,或者生命科学等相关背景,本科以上学历;
2. Well know the basic knowledge of ICH/GCP guidelines and obtain GCP training certificate. 熟悉ICH/GCP指南的基本知识,并取得GCP培训证书;
3. Be familiar with clinical trial procedures,through the company related SOP training and qualified with the related work; 熟悉临床试验相关流程,经过公司相关SOP培训后被认可可以执行相关工作。