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CareerCross uses cookies to enhance your experience on our websites. If you continue to view our sites without changing your browser settings, then it is assumed that we have your consent to collect and utilise your cookies. If you do not want to give us your consent, then please change the cookie settings on your browser. Please refer to our privacy policy for more information.
Location | Tokyo - 23 Wards |
Job Type | Contract |
Salary | Based on hourly rate |
Minimum Experience Level | Over 3 years |
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 |
求める経験とスキル:
・臨床開発関連資料の作成サポートまたはQC作成のご経験(日本語及び英語の同一資料間の内容に齟齬がないかなど)。
・マネージャーの指示を仰ぎながら、CROとの連絡窓口を担い、CROと円滑なコミュニケーションを取る。(最低CRA経験)
・指示待ち人間ではなく、自らアクティブ(将来発生する事項の察知や未処理案件を放置しない)に行動することができる。
・TOIEC 730点以上
・プロトコールなどの資料を作成した経験があるのが望ましい。
Job Type | Contract |
Salary | Based on hourly rate |
Hourly Rate | 2500~3000円 |
Work Hours | 月曜~金曜 09:00-17:30 |
Industry | Pharmaceutical |
Company Type | International Company |