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Mô tả công việc
Mô tả Công việc
· Oversight of regulatory submissions for assigned projects/countries, which may include completion of submissions or notifications, as required.
· Ability to read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
· Investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.
· Other duties as assigned.
Yêu cầu
Yêu Cầu Công Việc
· Can work at least 24 hours per week for a duration of 4 months to 6 months.
· Fresh graduates for senior students in related majors, such as biomedical engineering, biotechnology, pharmaceutical.
· Fluent in English is a must, in other language will be an advantage. Candidates who can speak Chinese will be a big plus.
· Ability to manage multiple projects, set priorities to meet deadlines.
· Keeping attention to details.
· Strong interpersonal skills, in written and oral.
· Basic skills in MS Office: Word, PowerPoint, Excel, Outlook.
Quyền lợi
Laptop
Phụ cấp
Đào tạo
Tăng lương
Thông tin khác
Bằng cấp:
Đại học
Độ tuổi:
Không giới hạn tuổi
Lương:
5 Tr - 8,5 Tr
VND
