Key responsibilities include:
- Selecting and training investigator sites, planning and organizing study meetings.
- Monitoring investigational sites to ensure protocol adherence.
- Ensuring timely enrollment of patients and clinical data accurate complete at sites.
- Processing CRFs, including data cleanup and classification of data.
- Collaborating with project manager in planning study conduct.
- Participating in the generation and finalization of SOPs and project management documents for clinical projects, and conducting training for CRO.
- 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
