Non-clinical safety researcher
塩野義製薬株式会社
- Safety assessment
- Non-clinical safety evaluation
- Drug discovery research
- Survival and reproductive toxicity tests
- Non-clinical safety pharmacology tests
- GLP tests
- in vitro cardiovascular evaluation
- Unexpected shape evaluation
- Pharmaceutical product development
- Japanese toxicology association certification
- Japanese Society of Toxicology certification
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Osaka
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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 recruitment of non-clinical safety researchers, business related to non-clinical safety evaluation from drug discovery research to non-clinical safety assessment application is conducted. We are looking for various meeting items from the establishment of non-clinical safety evaluation tests, such as survival and reproductive toxicity tests, non-clinical safety pharmacology tests, and the foundation research for new non-clinical safety evaluation tests, and various meeting items from each country's regulatory authorities. In addition, practical experience related to survival and reproductive toxicity tests, trustworthiness evaluation and GLP tests, and knowledge and practical experience related to in vitro cardiovascular evaluation and unexpected shape evaluation tests are required. Logical thinking and English communication skills are also required.Duties
In this job, business related to non-clinical safety evaluation from drug discovery research to non-clinical safety assessment application is conducted. Specifically, various meeting items related to non-clinical safety evaluation tests such as survival and reproductive toxicity tests, non-clinical safety pharmacology tests, and the foundation research for new non-clinical safety evaluation tests, and various meeting items from each country's regulatory authorities are included. In addition, practical experience related to survival and reproductive toxicity tests, trustworthiness evaluation and GLP tests, and knowledge and practical experience related to in vitro cardiovascular evaluation and unexpected shape evaluation tests, and the foundation knowledge of pharmaceutical development and English logical writing ability are required.Login to see all information about offers.
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