台北市內湖區5年以上碩士以上
1. Oversee the clinical study quality to ensure GCP compliance.
2. Plan and execute the co-monitoring activities
3. Perform the periodical QC review of Trial Master Files.
4. Develop and manage the study budget and timeline.
5. Preform the CRO selection and supervision.
6. Negotiate the site/CRO/vendor budget and contract terms.
7. Plan and execute the recruitment activities to boost site enrollment rate.
8. Organize regular/ad-hoc study meetings.
9. Organize Investigator meeting as needed.
10. Lead the preparation and review of protocol, ICF, subject materials.
11. Develop study-specific plans, instructions, manuals, and/or templates.
待遇面議