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PV Specialist
| Location | Tokyo - 23 Wards |
| Job Type | Permanent Full-time |
| Salary | 6 million yen ~ 10 million yen |
Job Description
- Work closely with the clinical operations and project management to ensure all drug safety activities are performed according to the regulatory and contractual requirements
- Support the appropriate Clinical Data Management (CDM) team(s) in the reconciliation of SAEs across safety and trials databases.
Client Details
Global CRO, leading in Asia-Pacific region and Japan with in-house diagnostic lab.
Description
- Contributes to the development and/or review of Clinical Trial Protocols, Case Report Forms and Adverse Event Reporting forms.
- Consistently responsible for assisting with the set-up of, and the provision of data to, Safety Committees / Drug Safety Monitoring Boards.
- Assist in the co-ordination of endpoint committees.
Job Offer
Development of a growing business unit directly under APAC. Career opportunities on a truly global scale.
Page Group Japan is acting as an Employment Agency in relation to this vacancy.
General Requirements
| Minimum Experience Level | No experience |
| Career Level | Mid Career |
| Minimum English Level | Fluent |
| Minimum Japanese Level | Native |
| Minimum Education Level | Bachelor's Degree |
| Visa Status | No permission to work in Japan required |
Required Skills
- relevant to pharmacovigilance/drug safety knowledge
Job Location
- Tokyo - 23 Wards
Work Conditions
| Job Type | Permanent Full-time |
| Salary | 6 million yen ~ 10 million yen |
| Industry | Bank, Trust Bank |
Job Category
- Medical, Pharmaceutical and Healthcare > R&D (Pharmaceutical)
