61 More detailed day-to day responsibilities will include:
83 Protocol development, protocol review,
83 support of the study set-up, review 30-40 documents on average including CRF, e-diary, lab manuals, data monitoring plan, …
83 during the study conduct: develop training materials for the Investigators and Ops teams,
83 review data
83 interact with the Authorities,
83 briefing documentations for the Authorities,
83 prepare clinical trials application materials,
83 may cover strategy level activities.

Requirement：
1. Above Master degree, prefer to PhD background;
2.Having experience with vaccines clinical development;
3.Pro-active, diligent, able to work independently and take ownership of their work