募集要項
- 仕事内容
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As a SAS programmer, you will be contributing to the all phases of clinical trials・You will play a key role in developing, implementing, and evaluating statistical programming standards and processes
・ You will closely work with the team members as well as external CRO partners to oversee and consult for the statistical programming deliverables and make sure consistency of approaches assigned to CROs.
・Review study and project related documents that requires statistical programming input.
・ Contribute to develop programming and quality standards
- 応募資格
-
- 必須
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・Needs to have deep understanding and experiences in oncology. (2-3 years aren't enough)
・Be able to work independently and confidently
・Business level English (Japanese isn't must)
- フィットする人物像
- Someone who can work independently and have a strong motivation/aspiration towards the challenging project/situations.
- 雇用形態
- Full time employee
- 勤務地
- Tokyo
- 年収・給与
- 800万円 ~ 1199万円
- 選考プロセス
- CV screening -> interviews x 3times