岗位职责:

1、协助项目经理完成试验核心文件的收集、整理、核查和归档；Assist the project manager in collecting, organizing, checking, and archiving the core documents of the trial.

2、协助项目经理收集试验相关信息，负责对临床试验进度做整体跟进、汇总及汇报；Assist the project manager in collecting relevant information for the trial, and be responsible for the overall follow-up, summarization, and reporting of the clinical trial progress.

3、跟进项目监查计划、重点问题处理的执行情况；Follow up on the implementation of the project monitoring plan and the handling of key issues.

4、协助项目组召集、组织网络及电话会议，组织、筹备、协调项目现场会议；Assist the project team in convening and organizing online and telephone meetings, and organize, prepare for, and coordinate on-site project meetings.

5、负责处理项目组其他行政工作；Be responsible for handling other administrative tasks of the project team.

6、完成上级经理分配的其他工作。Complete other tasks assigned by the supervisor.

任职要求:

1.本科及以上学历，临床医学、预防医学、临床药学等临床相关专业优先；Bachelor

s degree or above, with priority given to clinical-related majors such as clinical medicine, preventive medicine, and clinical pharmacy

2.熟悉药物临床试验管理规范（GCP）和临床工作相关法规，了解临床研究实施流程；Be familiar with the Good Clinical Practice (GCP) and relevant regulations for clinical work, and understand the implementation process of clinical research.

3.有良好的工作态度，工作严谨，有责任心，协调沟通能力强，有良好的团队精神与合作意识；Have a good work attitude, be rigorous in work, responsible, with strong coordination and communication skills, and possess good team spirit and cooperative awareness.

4.熟练应用电脑及办公软件；Proficient in computer operation and office software