1. MD with malignant hematology experience (doesn't have to be a Hematologist themselves) with experience covering medical monitoring responsibilities for registration enabling trials in Hematology/Oncology.
2. Fluent in English and Mandarin and on China timezone
3. General tasks/expectations: responding to sites, managing the day to day for the study, triaging complicated medical topics to line-manager, periodic data review/interpretation
4. Contributing to the FAQ log
5. Contrbuting to study amendments
6. Contributing to PI engagement efforts (as needed)
7. Contributing to eventual database lock process (data review) and inspection readiness
8. Attend study team meetings (remote is fine)