Clinical Operation Project manager 临床运营项目经理

1. Responsible for the project plan and timeline

2. Responsible for the budget of assigned trials 

3. Responsible for sites and vendors evaluation, selection and routine management 

4. To review and approve the project specific documents and tool forms

5. To lead study project meeting and mitigate all study issues 

6. To provide necessary training to all related staff of the trials

7. To oversight and coordinate all study daily routine work, including IM, recruitment, clinical monitor activities, AE/SAEs reporting, data management, statistics, clinical quality and compliance, etc. 

8. To manage the relationship of internally and externally, such as vendors and sites

9. To support the project NDA submission 

10. To support other teams as needed. 


1. Bachelor degree or above, medicine/pharmacology/biology is preferred  

2. At least 5 years clinical research experience, oncology/haematology area is preferred,

3. With project management experience, early development study experience is preferred

4. With ICH-GCP/GCP training 

5. With good communication skills

6. With good English skills (oral and writing)

7. With team work and problem resolve abilities

8. With good computer skills