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PV
| Hiring Company | 外資製薬メーカー |
| Location | Tokyo - 23 Wards |
| Job Type | Permanent Full-time |
| Salary | 6 million yen ~ 8 million yen |
Job Description
【求人No NJB2353465】
本ポジションは、医薬品や医療機器の安全監視プログラムの監督・監査を担当し、副作用報告の収集・評価・対応を行います。国内外の規制遵守を確保し、臨床試験や市販後調査の安全データ管理を支援。安全情報の報告やトレンド分析、関連部門との連携、規制動向の把握・対応、教育資料の作成、監査対応も含まれます。品質・報告の適時性を重視し、リスク管理に貢献します。
General Requirements
| Minimum Experience Level | No experience |
| Career Level | Mid Career |
| Minimum English Level | Business Level |
| Minimum Japanese Level | Native |
| Minimum Education Level | Bachelor's Degree |
| Visa Status | Permission to work in Japan required |
Required Skills
■Minimum Requirements:
・Work Experience:
Functional Breadth.
Collaborating across boundaries.
Operations Management and Execution.
・Skills:
Databases.
Employee Training.
Filing （Documents）.
Pharmacovigilance.
Reporting.
Safety Science.
・Languages :
English.
Job Location
- Tokyo - 23 Wards
Work Conditions
| Job Type | Permanent Full-time |
| Salary | 6 million yen ~ 8 million yen |
| Work Hours | 08:30 ～ 17:15 |
| Holidays | 【有給休暇】初年度 15日 1か月目から 【休日】完全週休二日制 |
| Industry | Pharmaceutical |
Job Category
Company Details
| Company Type | International Company |
