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Hiring Company | One of the world's largest pharmaceuticals company |
Location | Tokyo - 23 Wards |
Job Type | Contract |
Salary | 16 million yen ~ 20 million yen |
Planning:
Delivery:
Minimum Experience Level | Over 10 years |
Career Level | Mid Career |
Minimum English Level | Fluent (Amount Used: English usage about 75%) |
Minimum Japanese Level | Fluent |
Minimum Education Level | Bachelor's Degree |
Visa Status | Permission to work in Japan required |
• Act as central point of contact for vendor providing this service.
• Assist CPL with Interactions with CRO and site staff to adhere to study budgets.
• Requests accruals, and performs contract and invoice review.
• Participate in operation meetings with CRO, and cross-functional team members; document escalations and actions.
• Coordinate study team training in the investigator portal; monitor site/CRA user access and track compliance during the study.
• Coordinate with CPL and cross-functional team to assemble study documents as appendices for CSR at study close-out.
• Upon site closure, prepares subject files, inventories documents, reconciles document discrepancies, and organizes study files for electronic archive and off-site storage.
• SME for initiatives in conjunction with the CoE, as required to ensure consistent implementation
Job Type | Contract |
Salary | 16 million yen ~ 20 million yen |
Industry | Pharmaceutical |
Company Type | Large Company (more than 300 employees) - International Company |
Non-Japanese Ratio | About half Japanese |