Beijing KangChuanglian Biopharmaceutical Technology Research Co. LTD

Release Date：2024-07-15 Info. Source：Beijing Overseas Talents Center

Beijing Anti-Chuanglian Biopharmaceutical Technology Research Co., Ltd. is the research and development center of Shiyao Holding Group Co., Ltd. located in Beijing. Its business scope covers medical research and experimental development, technology development, transfer, consulting and service. The company has independent intellectual property rights and three authorized invention patents. The main research areas include cardiovascular and cerebrovascular, tumor, endocrine, neurological and psychiatric diseases, and the main research and development feature is the development of special preparations. Company registered capital of 5 million yuan, according to the regulations in Beijing Daxing District business tax.

Shiyao Holding Group Co., Ltd. is a national innovative enterprise integrating research and development, production and sales of innovative drugs.

At present, it has more than 10 drug production bases in Hebei, Shanxi, Shandong, Jiangsu, Jiangxi, Tianjin and other provinces and cities, and its products have been sold to more than 100 countries and regions around the world, with 36 varieties of single varieties selling more than 100 million yuan. Website address: http://www.e-cspc.com/about/index.html

NO.	Job Title	Professional Field	Specialization	Job Description	Qualifications	Age	Education	Number	Expected Starting Date	Working Months Each Year	Supportting Policy and Benefits	Valid Through	Target Country/Region or Organization for the Candidate
1	Senior Research Fellow in AI macromolecular drug design	Biomedical Science	Bioinformatics/Pharmaceutical Chemistry	1. According to the project requirements of protein acromolecules (antibodies, fusion proteins, peptides, etc.), make full use of computer aided design from scratch or develop new drug molecules based on existing molecular structures; 2. Familiar with the installation, use and maintenance of various computer-aided drug design software; 3. Tracking the latest trends of computer-aided drug design and timely introducing new technologies and methods; 4. Understand high-throughput screening techniques such as phage display or yeast display;5. Can predict and optimize the secondary structure of nucleic acid and optimize the sequence of nucleic acid 6. Complete other work arranged by the leader.	1. Major in structural biology, molecular biology or CADD, PhD, research direction is computer aided drug design; 2. Master the basic principles of computer-aided drug design and common biological information database;Familiar with molecular simulation, docking and other related software tools such as DS, MOE, able to independently complete the research and development work of computer molecular simulation, drug design and structure optimization. 3. Master the structure of macromolecular drugs such as amino acid properties, peptides and antibodies, and be able to independently design or transform macromolecules according to project requirements by using AI software;4. Innovative, have a certain understanding of immunology, and can put forward new ideas or suggestions for drug design based on knowledge of protein structure and AI design background; 5. Familiar with commonly used molecular biology tools and software; 6. Proficient in literature retrieval and reading in Chinese and English; 7. Have excellent teamwork spirit and dedication. 8. Committed to the development of biopharmaceutical industry, able to adapt to the fast-paced atmosphere of start-up companies and good pressure resistance.	Under 40 years old	Doctor	two	In July 2023	full-time	15 salary, dormitory, subsidies, group building activities	2024/12/31	unlimited	Send
2	Senior research fellow	Biomedical Science	pharmacy	1. Responsible for technological research of innovative pharmaceutical preparations;2. Connection between related projects and production system; 3. Prepare preparation process declaration materials, and cooperate with the completion of corresponding registration and declaration work.	1. Doctor degree, major in pharmaceutical preparation or related field; 2. Have strong professional knowledge of pharmaceutical preparation, familiar with the research points and quality attributes of pharmaceutical preparation.	Under 40 years old	Doctor	three	In July 2023	full-time	15 salary, dormitory, subsidies, group building activities	2024/12/31	unlimited	Send
3	kangdandan@cspc.cn	Biomedical Science	clinical trials	Be able to work independently or under the direction of line leader in the following areas: 1. Participated in clinical development projects as a representative of statistics department. Provide statistical leadership for clinical development projects, including conducting statistical design, and provide strategic support for other aspects of clinical development plans (CDPs) and target product profiles (TPPs). 2. Directly responsible for statistical integrity, adequacy and accuracy of clinical studies within the project, including cross-departmental cooperation with various functional departments in the study design, study implementation, analysis and reporting stages. 3. Deliver the following documents related to the research: The statistical part, statistical analysis plan, randomization scheme, data monitoring committee charter, clinical study report, and other documents required by the regulatory submission, such as comprehensive data summary, and statistical support for other research-related documents such as CRFs, DVPS, etc. 4. Keep abreast of the cutting-edge literature/technology progress of drug development projects in the field and related fields. 5. Support the development of standard operating procedures (SOP) of biostatistics department.	1. Biostatistics Manager: At least 2 years of working experience in a pharmaceutical and/or biotech company is required for a PhD degree (5 years for a master's degree); Senior Manager, Biostatistics: A Ph.D. degree requires at least 3 years (6 years for a master's degree) of work experience in a pharmaceutical and/or biotech company. 2. Solid knowledge of mathematics and applied statistics. 3. Good English writing and interpersonal skills in a business environment. 4. Proficient in using statistical software such as R and SAS. 5. Familiar with clinical study design, clinical data analysis, including statistical procedures in analysissoftware. 6. Understand the statistical analysis methods, results and presentation forms of clinical data. 7. Familiar with regulatory regulations and guidelines. 8. Understand clinical trial design and reporting processes, as well as regulatory reporting requirements, including electronic data submission and CDISC implementation requirements. 9. Experience in writing statistical analysis plans, study protocols and clinical study reports is a must.	Under 40 years old	Doctor	0ne	May 2023 - June 2023	full-time	Support household registration, annual free medical check-ups, meal allowances, and team building	2024/12/31	unlimited	Send

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