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Pharmacology and Toxicology Researcher

Shenzhen China
Responsibilities

1.Responsible for the preclinical pharmacodynamics of new drug development, Toxicology and pharmacokinetics and other related data collation, the development of new drug development pharmacology and toxicology development program, participate in animal testing in animal centers.

2.Responsible for CRO research, implementation of relevant research, tracking the progress of the trial, and analysis and summary of the trial results.

3.Responsible for the study protocol. Review and approval of study protocols, summary reports and other related technical information.

4.Responsible for the translation and writing of the pharmacology and toxicology part of the new drug application materials, and cooperate with the registration, CMC and clinical staff to complete the work related to the new drug application.

Qualifications

1.Bachelor's degree or above, in pharmacology. Toxicology or other related professional background,

2.Familiar with national technical review requirements and national drug management regulations (NMPA & FDA) and ICH guidelines.

3.Should be able to translate English literature and Chinese reports.

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