First-level areas：Biotechnology
First-level areas：Biopharmaceutical technology
Source：Social Recruitment
Job description ：
Job description.
1. Responsible for completing safety and toxicology testing plans for various projects in collaboration with CRO companies, ensuring standardized and efficient completion of experiments and data collection;
2. Research the toxicological issues that arise during clinical development of the project and explain their mechanisms;
3. Continuously improve personal professional skills and complete other assigned tasks.
Job requirements.
1. Educational requirements. PhD;
2. Professional requirements. related majors such as medicine, biology, pharmacology, toxicology, etc;
3. Work experience. More than 1 year of work experience;
4. Ability requirements. Possess certain drug research and development experience or have conducted preclinical safety evaluation tests under GLP conditions, familiar with toxicology related policies and regulations; Have good experimental operation skills; Diligent and hardworking, with a strong sense of responsibility; Have a certain level of proficiency in listening, speaking, reading, and writing in foreign languages (English);
5. Language requirements. Good English reading, Chinese communication, and writing skills.

Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: ‘Name + Position + Company Name + Location’.