Job Description
Support regulatory affairs daily work
Responsibilities
Responsibility:
Assist RA Lead to research on overseas and local policy, regulation and technical guideline in field of Genetherapy and Cell therapy.
Schedule the relevant meetings/workshops and seminars, arrange the logistics and record the meeting minutes.
Assist RA lead to write and complete the final research report.
Commercial Intelligence searching and summary
Qualification Required
Bachelor degree and above in life sciences or relevant scientific background.
Knowledge of ICH Guidelines, local regulations, and GXPs is preferred
Be familiar with the registration dossier.
Good learning, analytical and issue identification abilities, and attention to detail
Creative problem solver and keen ability to address current and anticipated issues
Good computer skills in EXCEL and WORD
Good level of English language (spoken /written)