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Regulatory Affairs for drug development

塩野義製薬株式会社

  • Pharmaceutical development
  • pharmaceutical regulations
  • Pharmaceutical strategy
  • pharmaceutical consultation
  • pharmaceutical experience
  • global application experience
  • English and Japanese communication ability
  • Work Location Tokyo
  • Company employee count 1,001 to 10,000

Company Info

Sumitomo Pharmaceuticals aims to create a new platform in 2030 to create the future of health care. As a data engineer, you will collect and manage internal and external data, establish a data management system at the company-wide level, and develop plans and strategies related to data utilization in the healthcare domain, including business plans and expansion strategies.

Job Summary

In the position of Regulatory Affairs for drug development, we will implement pharmaceutical strategy in Japan and Asia, and promote development projects, as well as refer to pharmaceutical strategy and promote development projects. Experience in pharmaceutical strategy and evaluation work at the company and experience in English and Japanese communication ability are required, and knowledge and experience in pharmaceutical regulations in the United States and Europe are desired.

Duties

As a member of the drug development team (watching and fighting agents, etc.), we will implement pharmaceutical strategy in Japan and Asia, and promote development projects. We will also conduct research on pharmaceutical strategy for appropriate development projects in Japan, and implement consultation with various national regulatory authorities and pharmaceutical development in each country. As a skill that can be obtained, it is possible to independently conduct consultation with various national regulatory authorities and development in Japan and Asia, based on knowledge of pharmaceutical regulations and experience in English and Japanese communication.

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Regulatory Affairs for drug development

塩野義製薬株式会社

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