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| Hiring Company | 外資スペシャリティファーマ |
| Location | Tokyo - 23 Wards |
| Job Type | Permanent Full-time |
| Salary | 6 million yen ~ 9 million yen |
【求人No NJB2353782】
本ポジションは、臨床試験の開始から維持、終了までの活動をリードし、ICH/GCPや社内規定、地域規制に準拠した高品質な遂行を担います。申請戦略の策定やIRB・規制当局への提出書類作成、契約交渉、サイト選定・立ち上げを効率的に推進。問題の早期発見・解決やプロセス改善にも積極的に関与し、社内外の関係者と良好な関係を築きながら、後輩の指導も行います。
| 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 |
【Qualification Required】
Education Required:
Bachelor’s degree or higher in a scientific or healthcare discipline. Experience may discretionarily substitute for degree.
Computer Skills:
Intermediate skils in Microsoft Office ・ Outlook Word Excel PowerPoint Teams SharePoint
【Other Qualifications】
■At least 2 years experience in a similar role
■Fluent in local language/s as well as written and verbal English ・・
■Strong interpersonal skills can do attitude and problem solving skills
■Able to multi task and meet compressed timelines Knowledge in the execution of clinical trials understanding of ICH/GCP
■Prioritization of tasks in the achievement of goals
■Highly organized
■Diligence in follow through
| Job Type | Permanent Full-time |
| Salary | 6 million yen ~ 9 million yen |
| Work Hours | 09:00 ~ 18:00 |
| Holidays | 詳細は求人ご紹介時にご案内いたします。 |
| Industry | Pharmaceutical |
| Company Type | International Company |