First-level areas：Biotechnology
First-level areas：Bioinformatics Technology
Source：Social Recruitment
Job description ：
Duty.
1. Comply with GLP requirements and be fully responsible for the management of toxicology and pharmacology topics;
2. Responsible for designing and conducting preclinical reproductive toxicology trials, ensuring that the trial protocol is approved by the client, and coordinating with various departments to arrange the trials;
3. Supervise the operation of each stage of the experiment, ensure that the experiment is carried out according to the experimental plan, and ensure that the experimental process complies with GLP regulations;
4. Resolve relevant issues that arise during the experiment, supervise the collection of experimental data, and inspect the experimental data;
5. Prepare the experimental summary report and be responsible for its scientific validity;
6. Responsible for timely and effective communication with the client.
Job requirements.
1. Major in animal medicine, veterinary medicine, medicine, or related fields, with a focus on reproductive research and a doctoral degree
2. Proficient in English listening, speaking, reading, and writing;
3. Familiar with basic animal experimental procedures, proficient in using office software and statistical software;
4. Good learning ability and team spirit, with good coordination and management skills;
5. English CET-6 or above, with excellent listening, speaking, reading, writing, and communication skills;
6. Priority will be given to those who have published relevant academic papers.

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’.