Vị trí công việc này hiện tại đã hết hạn nộp hồ sơ, bạn có thể tham khảo thêm một số công việc liên quan phía dưới
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
• Can work at least 24 hours per week for a duration of at least 4 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
• Allowance: VND 50,000/hour.
• Confirmation on completing the internship.
• Have chance to become a full-time employee.
• Professional, dynamic working environment.
Working time: 8:00-17:00, Monday-Friday
Thông tin khác
Mức lương
Trên 4 triệu
Số lượng tuyển
1 người
Hình thức làm việc
Thực tập
Cấp bậc
Thực tập sinh
Giới tính
Không yêu cầu
Kinh nghiệm
Không yêu cầu kinh nghiệm
