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Responsibilities
- Be responsible in completing target validation, data collection, project investigation, etc.;
- It is preferred to be able to establish various in vitro experiments, such as compound screening, target binding, molecular interaction, CRISPR, etc.;
- It is preferred to be able to establish various in vivo tumor models, such as subcutaneous model, immune oncology model;
- Be responsible for putting forward guiding opinions on the research of in vivo and in vitro efficacy;
- Be responsible for coordinating the progress of research, and promoting the project pipeline.
Requirements
- PHD/ or MD with 3 years of working experience; Research paper with IF > 5 is preferred;
- Major in molecular biology, cell biology, and other biology related majors;
- PHD (Year 1)/ or MD with 3 years of working experience;
- Research paper with IF > 5 is preferred;
- Major in molecular biology, cell biology and other biology related majors;
- Practical operation experience is preferred, such as cancer cell and immune cell co culture, ELISA, WB, qPCR, HTRF, CTG, etc.; Master the analysis and processing of experimental data;
- Familiar with drug research and development process, and have relevant experience in the evaluation of immune targets and antitumor drugs;
- Comprehensively understand the development trends of industry technology, and be able to grasp the development direction of cancer research;
- Good English expression ability, strong organization, management, and coordination ability;
- Understand the development trend of industry technology, and be able to grasp the development direction of cancer research;
- Good English expression ability, strong organization, management, and coordination ability.