1. Develop and review the case report form (CRF). 2. Develop and review the database specification. 3. Develop and review the database structure on the database builder. 4. Develop and review the data validation specification. 5. Conduct the database validations including the user acceptance testing. 6. Develop and maintain the CRF library. 7. Develop and maintain the edit checks (ECS) library. 8. Develop and conduct the data review process and dummy data generation. 9. Oversee and coordinate clinical data integration activities as a DMPM. 10. Develop and update the templates of related processes. 11. Develop and manage the working process and standard operating procedures (SOPs). 12. Act as a mentor for the Associate Clinical Data Scientist I 13. Complete other tasks or assignments requested by the Supervisor.
待遇面議
(經常性薪資達 4 萬元或以上)
1. Good English written, listening, verbal communication skills. 2. Familiar with the clinical data structure. 3. Familiar with the Good Clinical Data Management Practice (GCDMP). 4. Familiar with the Good Clinical Practice (GCP). 5. Ability to work both independently and collaboratively with a team in a cross-cultural, and geographically dispersed environment. 6. Good communication skills to coordinate with the project team. 7. Good knowledge and skill in Microsoft Office and other IT tools. 8. Strong analytical mind and skills.
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