募集要項
- 募集背景
- A leading drug development services company is searching for an individual with experience in the pharmaceutical industry and deep regulatory knowledge to join them as the Regulatory Submissions Manager. This is an exciting opportunity to use your talents as a member of a global institution.
- 仕事内容
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Responsibilities:
* Submit appropriate documentation to regulatory authorities globally prior to the performance of clinical trials
* Submit documentation prior to pharmaceutical marketing initiatives
* Act as a liaison between the client and regulatory authorities
* Interact proactively with all levels within the company and client organizations; assist other staff with business development activities related to regulatory submissions
Requirements:
* Bachelor's degree or equivalent in pharmacy or a life sciences field
* 5+ years' experience in the pharmaceutical industry with 3 years' regulatory affairs or drug development experience preferred
* Direct supervisory and project management skills and an ability to work independently
* An understanding of governmental regulatory processes and regulations related to drug regulation
- 応募資格
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- 必須
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・Bachelor's degree or equivalent in pharmacy or a life sciences field
・5+ years' experience in the pharmaceutical industry with 3 years' regulatory affairs or drug development experience preferred
- 雇用形態
- Permanent
- 勤務地
- Tokyo
- 年収・給与
- JPY8000000 - JPY12000000 per annum + 800万円ー1200万円
