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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 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 languages 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.
Hình thức
Quyền Lợi
- Allowance: The hourly rate ranges from VND 40,000 to 50,000, depending on ability.
- Confirmation on completing the internship.
- Have chances to become a full-time employee.
- Professional, dynamic working environment.
Mức lương
Từ 4 đến 9 triệu
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hãy phản ánh với chúng tôi.
Tham khảo: 10 Dấu hiệu nhận biết hành vi lừa đảo qua tin tuyển dụng.
Tham khảo: 10 Dấu hiệu nhận biết hành vi lừa đảo qua tin tuyển dụng.
