Job Responsibilities:

1. Based on the research project and clinical characteristics, take responsibility for in-depth studies of the pharmacological mechanisms underlying the project; design protocols for the trials you oversee, as well as handle, analyze, and interpret the associated data.
2. Undertake the establishment of in vitro and in vivo drug screening models for the company's new drugs, as well as activities screening and efficacy evaluation tasks.
3. Responsible for organizing and drafting the pharmacology section of new drug registration documents, as well as conducting and compiling literature searches.
4. Collect, analyze, and research information on domestically and internationally listed or pipeline drugs, providing technical literature support, as well as conducting indication surveys and analytical studies.
5. Assist in publishing academic papers, provide pharmaceutical research support to the market, and enhance the company's academic influence.

Job Requirements:

1. PhD degree in pharmacology, molecular/cellular biology, or immunology; previously responsible for conducting systematic preclinical pharmacological studies of drugs.
2. Proficient in retrieving and querying relevant foreign drug research materials related to pharmacology and toxicology studies;
3. Possesses strong analytical and problem-solving skills; robust learning and practical abilities; and excellent English proficiency in listening, speaking, reading, and writing.