Key responsibilities include:

1. Selecting and training investigator sites, planning and organizing study meetings.
2. Monitoring investigational sites to ensure protocol adherence.
3. Ensuring timely enrollment of patients and clinical data accurate complete at sites.
4. Processing CRFs, including data cleanup and classification of data.
5. Collaborating with project manager in planning study conduct.
6. Participating in the generation and finalization of SOPs and project management documents for clinical projects, and conducting training for CRO.
7. Participating in Managing and select Contract Research Organization (CRO) and other vendors
   Experience:

The ideal candidate should possess a minimum of 2 years of experience in clinical research monitoring.Experience with oncology diseases and CAR-T cell products clinical trials highly desired but not absolutely necessary