募集要項
- 仕事内容
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• Develop strong site relationships and ensure continuity of site relationships through all phases of trial.
• Perform clinical study site management/monitoring activities in compliance with Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
• Gain an in-depth understanding of the study protocol
• Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
• Participates & provides inputs on site selection and validation activities.
- 応募資格
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- 必須
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At least 5 years of CRA experience
5 Years of Oncology experience
High Business English
Native Japanese
- 雇用形態
- Permanent
- 勤務地
- 東京都
- 年収・給与
- 700万円 ~ 1000万円