Sinocelltech Group Limited

Release Date：2024-02-07 Info. Source：Beijing Overseas Talents Center

Since the establishment of Shenzhou Cell Engineering Co., Ltd. under the Group in 2002, the company has long adhered to independent research and development and self -master core technologies, has established a full set of technology platforms for biopharmaceuticals and vaccines, and independently developed a competitive rich product pipeline, covering coverage Malignant tumors, autoimmune diseases, genetic diseases, and disease prevention. In July 2021, the company lasted for 14 years. The first domestic reorganized coagulation products (Anjiayin®), which was treated with rare diseased hyperactivity disease treatment, realized listing and sales. At the end of August 2022, the company's first antibody drug and the first anti -tumor product Ripupozab (Anpingxi®) was approved to be listed. In December 2022, in March 2023, the company's independently developed reorganized new crown virus (Alpha/Beta mutant strain) S SCTV01C (Anno Neng® 2) and its iterative product reorganization of new crown virus 4 prices ( Alpha/Beta/Delta/Omicron) S trimer protein vaccine SCTV01E (Anno ®4) has been incorporated into the country into emergency use.

The company's management team has rich experience in research and development and production of biopharmaceuticals. Dr. Xie Liangzhi, the founder of the company, was a doctorate in MIT at the Massachusetts Institute of Technology, and successfully tried the animal cell flow plus cultivation technology controlled by complex, variables and associated chemical measurement methods. In 1994 By the leading level of 2,400 mg/liter, it laid an important foundation for the large -scale production of antibody drugs; after returning to China in 2002, it assumed a number of national "863" plans, and the national "new drug creation" major topic topics; led the team to establish the international international The first-class biopharmaceutical research and development and industrialization technology platform has broken through a series of key technologies, overcome high-difficult biopharmaceutical production technology such as reorganized coagulation, long-term interferon-β, and 14-valent HPV vaccine; the company's deputy general manager Wang Yang Doctors have more than 20 years of experience in the research and development and project management of vaccines and antibody drugs. They have led the quality analysis and quality standards of cervical cancer vaccine. They are internationally renowned biopharmaceutical control experts.

The company's production bases located at the Beijing Economic and Technological Development Zone Headquarters are all constructed in accordance with the CGMP standard. Among them, the first phase of the project has been built in the 12,000 -liter original liquid production line that can realize commercial production; The remaining two raw liquid production lines of the same scale are under construction. The company obtained the "Drug Production License" in July 2018, and the new vaccine production license was added at the end of May 2022.

The company first publicly issued shares on June 22, 2020 and was listed on the Shanghai Stock Exchange Science and Technology Board.

No.	Specialization	Job Title	Number	Valid Through	Job Description	Age	Education	Qualifications	Supportting Policy and Benefits	Target Country/Region or Organization for the Candidate
1	Major in biomedicine	Research and development of macromolecular biological drugs	1.0	2024/12/31	1.Formulate the company's technology strategy according to the company's strategy, grasp the industry's cutting-edge technology and development direction, implement and supervise the implementation of technology research and development and implementation of long-term and short-term strategies, supervise the technology research and development activities, and provide guidance and check on specific technical issues;2.Overall management of the company's R&D and technology development, responsible for the overall operation at the technical level, including R&D project approval, project implementation, project transfer and technical data management; To plan the company's technological development route and the development of new products and new technologies, to achieve the company's technological innovation goals, and to timely understand and supervise the implementation of the technological development strategy plan; Ensure the market leadership of the company's technology, products and solutions, and lead the company's technological development direction and technological progress;3.Participate in the decision-making of major technical projects, guide and review the overall technical plan of the project, and evaluate the quality of each project; Coordinate the relationship between R&D department and other departments, maintain company unity and efficient collaboration;4.Responsible for process development, verification and scale-up, development and optimization of serum-free culture medium for mammalian cells, cooperate with the cell culture process team to complete process development and scale-up, and solve culture-related problems; Solve process problems encountered during process development, and predict and raise potential problems of unimplemented projects; Complete the company's R & D tasks and be responsible for the results;5.Guide the writing, sorting out and reviewing of registration application materials and original records as well as the corresponding on-site verification in the registration application. Promote project implementation and provide guidance to relevant R&D personnel;6.Presided over the establishment and improvement of R&D management system and related working procedures, promoted and supervised the implementation of the system and working procedures.7.Cultivate the company's technical team, supervise and guide the work of the technical department, and build a high performance technical team.	Under 55 years old	Doctor	1. PhD degree, molecular biology, cell biology, biochemistry and other disciplines;More than 15 years of experience in new drug development and management in biopharmaceutical industry, served as the R&D leader of a large biopharmaceutical company, understand the latest research trends and progress of the international and domestic industries related to biopharmaceutical research and development;3. Excellent management, coordination and communication skills (capable of managing a team of 100 people), brave in innovation;Can work steadily in Beijing, China.	1. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
2	Major in biomedicine	Vice President of Business Development	1.0	2024/12/31	1. According to the company's strategic development needs, responsible for looking for cooperation opportunities with domestic and foreign organizations, research institutions, well-known and innovative pharmaceutical companies;2. Responsible for collecting and sorting out medical information at home and abroad, implementing the screening of potential target projects, conducting project initiation research on target projects, writing and submitting project feasibility evaluation reports, coordinating and organizing the convening of project initiation review;3. Mainly responsible for the selection and docking of the company's external innovation projects, foreign cooperation or market development (including but not limited to project and company search, market research, evaluation and business negotiation);4. Responsible for potential customer contact, business negotiation of expansion projects, deal with obstacles in the cooperation process, promote cooperation, and ensure the timely promotion and completion of projects;5. Study the latest trends of the market and industry, explore the development direction of the pharmaceutical industry, grasp the domestic and international pharmaceutical market trends and potential products, businesses and latest trends.	Under 55 years old	Master	1. Major in medicine, master degree or above, more than 10 years of BD experience in the pharmaceutical industry, familiar with the operation of business development module;2, familiar with domestic and foreign pharmaceutical enterprises, market status and development trend of strong market sensitivity, information capture ability and development ability, in the industry has a good relationship and communication network;3, good at business negotiation, have overseas study or work background, English can be used as the working language.	2. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
3	Major in biomedicine	Computer-Aided Drug Design	1.0	2024/12/31	1. Engaged in research and development of computer molecular simulation, drug design and structural optimization.2. Skilled professional drug design software can use various types of CADD software to elaborate relevant drug targets and the binding mode of drugs and proteins, and propose the direction of drug design according to the binding mode to guide the design and structure optimization of innovative drugs;3, proficient in homologous modeling technology;4. Organize or participate in related scientific research projects and activities organized by the company;5. Cooperated and communicated well with other departments to ensure the smooth progress of the project.	Under 40 years old	Doctor	1, Major in computational chemistry or CADD or related major, doctoral degree, research direction is computer-aided drug design, relevant work experience is preferred;2. Good bilingual reading and writing skills in Chinese and English;3, solid basic knowledge, strong scientific research ability, love scientific research work, work initiative, careful and cautious, strong sense of responsibility, good professional ethics, team spirit, strong interpersonal communication skills;	3. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
4	Major in biomedicine	Biological drug structure researcher	1.0	2024/12/31	1. Responsible for protein computer modeling, structure prediction/analysis and basic information analysis: conduct rational/semi-rational structural optimization design for egg self according to the analysis results and confirm the plan.2. Responsible for the preliminary screening of protein crystallization conditions, crystal line data analysis and structure analysis.3. Analyze and evaluate the developability of self-contained drugs and control and optimize drug risk items to meet process and clinical requirements.4. Cooperate with team to complete project design, implementation and summary according to project planning and strategy.5. Follow up the most cutting-edge research results in the field, build a new protein structure analysis platform, and develop new drug design, transformation, optimization and analysis methods.6. According to the design scheme, write the relevant scheme test plan and complete the corresponding technical report.7. Prepare application materials and public literature related to drug structure and molecular design.	Under 40 years old	Doctor	1. Education requirement: Doctor's degree or above.2. Major requirements: Virology, structural biology, biophysics, bioinformatics, etc.3. Other requirements: familiar with protein structure, skilled application of various structural analysis software; Good communication and teamwork skills, strong sense of responsibility.	4. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
5	Major in biomedicine	Bioinformatics researcher	1.0	2024/12/31	1. Make full use of bioinformation analysis, statistical analysis and computational biology analysis tools to complete bioinformation analysis (including genome, transcriptome functional analysis and multi-omics integration analysis), organize and write reports;2. Provide bioinformatics data analysis support for the company's new drug research and development project, and be responsible for the bioinformation analysis of high-throughput sequencing data, result interpretation, model establishment, and development and optimization of data mining methods;3. Use bioinformatics database and clinical information related database for data mining, data analysis and result interpretation; Follow up public biometric information databases and analyze software trends4. Work with clinical and translational medicine teams to provide bioinformatics support for the screening of molecular markers and indications for drug candidates at the clinical stage;"	Under 35 years old	Master	1, Bioinformatics, systems biology related major, master degree or above;2, skilled use of classic biological information tools; Master biological information related database retrieval;3, omics research experience, clinical multi-omics project is preferred4, have strong scientific research ability, familiar with Perl/Python/R/Java and other more than 1 programming language; Master Benchling, Vector NTI, IGV, IPA, Graphpad, MobaXterm and other software;5, work actively, strong sense of responsibility, team spirit, service awareness and good communication skills	5. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
6	Biostatistics, Statistics	Drug discovery researcher	1.0	2024/12/31	1. Conduct research on the development of new drugs for the company's projects; Multi-technology platform cutting-edge technology research and development,2. According to the research and development goals of the project, targeted research programs, including drug structure, molecular technology, cellular level, screening of candidate molecules, design of experimental programs, and completion of experiments, data analysis and report writing on various technical platforms;3. Communicate with other departments, promote new drug application, and participate in the writing and sorting of pharmacological part of new drug application materials;	Under 35 years old	Master	1. Education requirement: Master's degree or above2, Major requirements: Cell biology, biochemistry and molecular biology, immunology and other related majors3. Other requirements: Strong learning ability, thinking ability, rigorous and dedicated work attitude, excellent teamwork and communication skills. Proficient in relevant professional theoretical knowledge, rich experimental experience and strong analytical ability, with good English reading ability and literature review ability	6. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
7	Clinical Medicine Science	Process development researcher	1.0	2024/12/31	1. Process development and research of cell biology/purification/formulation platform for drug and vaccine projects2, literature research, design process development experimental scheme, write SOP, process regulations, application materials, etc3. Summarized and analyzed the data, updated the plan and explored, developed and optimized the process conditions4, cooperate with upstream and downstream departments to complete the project process evaluation and sample preparation, and cooperate with pilot test to scale up the production process.	Under 35 years old	Master	1, master degree or above, biology, medicine and other related majors2. Have a solid basic knowledge of biology, master methods and principles, and have the ability of experimental operation, analysis and problem solving3, positive and optimistic personality, serious and responsible work, team spirit, good communication and execution ability	7. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
8	Major in biomedicine	Director/Deputy Director of Statistics	1.0	2024/12/31	Job responsibilities:1. Assist the clinical team to establish and implement the strategic development of biometrics, establish SOP and related quality management system;2. Provide the company's senior management, medical and clinical operation teams with advice on the latest biometric methods and tools for drug development;3. Design a clinical research plan to ensure that it is clinically and statistically effective;4. Provide data and biostatistics support for the clinical research team, and assist the clinical programming team to prepare forms, lists and data to ensure compliance with regulatory requirements;5. Communicate with regulatory agencies as a biostatistics expert on behalf of the company.	Under 45 years old	Master	1. Master or PhD in statistics;2. With more than 8 years of pharmaceutical company, global pharmaceutical company biostatistics experience and CRO experience is preferred;3. Experience in phase I-III clinical trials, tumors and vaccines are preferred;4. Work experience in CDISC compliance, solid knowledge of GCP and global regulatory statistical guidelines;5. Good communication and interpersonal skills.	8. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
9	Major in biomedicine	Medical Director	1.0	2024/12/31	1. As an expert in the medical research field of the company, lead or participate in medical related activities both inside and outside the company.1) Guide and participate in the design of phase I, II, III, and IV clinical trials for the company's research and development projects, providing high-quality clinical data for project decision-making;2) Participate in, guide and review the writing of medical related content in the company's R&D project application materials (such as IND/CTA, BLA/MAA, etc.);3) Establish and maintain communication channels with government regulatory authorities, industry associations/associations, medical experts involved in our company, research institutes, and other relevant departments, track the latest regulations and domestic and foreign medical progress, and help enhance the company's industry awareness and influence;4) Evaluate the development direction of newly developed drugs in the medical field, as well as their application prospects in the market, and assist in the research and development or introduction of new projects; Pharmacological and toxicological research plan and result evaluation;5) As a member of the company's scientific committee, participate in the decision-making of major medical technical solutions related to new drug research and development, the formulation of medical plans, and the leadership and review work of summary reports;6) Responsible for preclinical pharmacological and toxicological research, responsible for high-level academic exchanges with academic authorities and VIP experts in related fields, understanding the clinical demand for new drugs, and cooperating with the R&D department to develop strategies that are conducive to new drug development;7) Coordinate collaboration with various functional departments of the company;8) Complete other tasks assigned by the leader.2. As a core member of the medical department, lead and participate in the medical management of clinical trial projects.1) As a core member of the Medical Department, lead and participate in the medical related management of clinical trial projects;2) Responsible for reviewing and revising the overall clinical research plan and project data (project/annual/monthly) for each project;3) Responsible for maintaining relationships with VIP medical experts;4) Responsible for providing the final medical opinion on disputes arising from serious adverse events or other reasons in our company's clinical trials or marketed products; Responsible for the medical review of adverse drug reaction reports.3. Team management.1) Responsible for establishing departmental management systems and approving relevant documents;2) Responsible for department performance evaluation and cost management;3) Develop and implement personnel recruitment and training plans for the team, and build and maintain an efficient, professional, and hierarchical project execution team;4) Develop and supervise the implementation of various administrative regulations within the team.	Under 45 years old	Master	1. Educational requirements: Doctorate or Master's degree in Clinical Medicine2. Professional requirements: More than 5 years of clinical work experience in hematology oncology specialty.3. Foreign language requirements: Proficient in consulting, reading, and translating relevant professional literature; Fluent in spoken language.4. Work experience:1) ≥ 4 years of relevant work experience in drug clinical research, with work experience in the field of hematology and oncology being an added bonus; 2) Having experience in designing clinical trials of different stages and experiencing all stages of clinical trial operations. Experience in personally participating in Phase I clinical trials of cancer drugs is an added factor;3) Having experience in writing medical related drug declaration materials and dealing with different drug administration departments;4) More than 3 years of successful management experience in a team of ≥ 5 people;5. Knowledge requirements:1) Very solid knowledge of clinical medicine;2) Strong knowledge of clinical oncology and clinical immunology;3) Familiar with the entire process of drug development and global drug development;4) A certain level of knowledge in clinical pharmacology, drug vigilance, and pharmacogenetics;5) Familiar with GCP and project management;6. Skill requirements: Strong affinity; Good communication and presentation skills; Strong organizational and coordination skills; The ability to successfully lead cross departmental teams or multi departmental organizations;7. Quality requirements: Strong initiative;8. Emphasize strategy, time management, and results;9. Possess team spirit.	9. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
10	Major in biomedicine	Senior Researcher in Quality Research	1.0	2024/12/31	Job responsibilities:1. Responsible for the development or optimization of relevant methods;2. Responsible for the introduction of new methods and technologies;3. Responsible for sample testing and analysis, result determination standards;4. Responsible for equipment procurement and maintenance;5. Responsible for data writing.	Under 40 years old	Doctor	Qualifications:1. Major in biology, chemistry, pharmacy, etc., doctor degree;2. Ability to track new technologies and new methods, strong acceptance ability and strong innovation ability;3. Have excellent experimental operation ability, rich theoretical and practical experience in liquid phase, mass spectrometry, Elisa and other analytical means, have a certain understanding of the field of biological drugs, and have a strong ability to find problems and solve technical problems;4. Professional English and Chinese book writing ability;5. Strong ability of experimental design, arrangement and implementation;	10. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
11	Major in biomedicine	Deputy Director of R&D Quality	1.0	2024/12/31	Job responsibilities:1. Responsible for research related to formulation development;2. Responsible for the quality research of therapeutic monoclonal antibody drugs, recombinant protein drugs and vaccines (development, establishment and verification of methods for primary structure, advanced structure, physicochemical properties and biological activities, etc.);3. Keep abreast of advanced analysis methods or research and development trends at home and abroad, and put forward guidelines for the department's work;4. Responsible for solving technical problems encountered in quality research and guiding subordinates to carry out quality research;5. Responsible for communicating and responding to technical content related to quality research with regulatory agencies;6. Responsible for the preparation of quality declaration materials, communication materials and promotion of registration and declaration for domestic and foreign projects.	Under 45 years old	Doctor	Job Requirements:1. Doctor degree or above, major in pharmacy, analytical chemistry, biological analysis, biochemistry or related;2.7 years of antibody and protein drug quality research experience, including more than 5 years of management experience, recombinant protein, antibody and other quality research related work experience is preferred;3. Familiar with the biological analysis, physicochemical analysis, impurity analysis and other technologies involved in quality control of recombinant protein and antibody drugs, as well as the content regulations of preclinical analysis;4. Familiar with the Chinese pharmacopoeia and the general principles of quality control analysis methods and verification technology for biological products and chemical drugs, familiar with the relevant regulations of FDA, EU and ICH on biosimilar drugs.5. Good background in biopharmaceutical research and development and English reading and writing ability;	11. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
12	Major in biomedicine	Head of mass spectrometry research	1.0	2024/12/31	Job responsibilities1. Responsible for the establishment, application and implementation of the company's mass spectrometry research projects;2. Led the team to introduce new technologies and methods related to mass spectrometry, and coordinated the establishment or optimization of analytical methods and confirmation of completion methods to meet the analysis and testing needs of various projects;3. Responsible for the analysis and detection of samples in the early stage of research and development or process optimization, and provide data support for the evaluation of drug properties and process optimization of candidate samples;4. Solve various problems in the process of analysis method development, optimize and confirm existing analysis methods, summarize or review analysis method development data and report;5. Responsible for the preparation and review of technical documents.	Under 45 years old	Doctor	Job requirements1. Doctor degree or above, major in biology, chemistry, pharmacy or related;2. Have working experience in the macromolecular biologic drug industry in pharmaceutical companies, familiar with the general mass spectrometry analysis methods and principles of biological macromolecules;3. Rich experience in mass spectrometry theory and practical operation;4. Proficient in reading English literature, CET-6 or above.	12. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
13	Major in biomedicine	Vice President of Quality Management	1.0	2024/12/31	1. Responsible for the formulation and implementation of the global market -related quality strategy, quality policy, and quality goals;2. Responsible for the establishment and improvement of the company's quality management system in accordance with the current regulations requirements of various countries, and ensure that all activities in the life cycle of research and development, production, inspection, non -clinical, clinical trials, and marketization meet the requirements of all domestic and foreign regulations;3. Responsible for the establishment, improvement and implementation of the company's GXP training management system, and to promote quality strategies;4. Establish a quality risk assessment and management system to correct the quality management system of preventive systems, data integrity management systems, supplier review management systems, adverse reaction report systems to ensure the effectiveness of its implementation;5. Responsible for organizing the company's internal self -inspection and acceptance of external audits, coordinating the various departments of the company to cooperate with the inspection, and implement the rectification that does not meet the items;6. Review and approval standard operating procedures, deviation reports, stability research plan reports, production inspection, verification plans and documents, instrument and equipment monitoring and maintenance plan and other quality related documents;7. Responsible for the release of materials and products to ensure the compliance of the release procedure; be responsible for evaluating and approved material suppliers, and responsible for the management of suppliers and formulating the annual audit plan of the supplier;8. Responsible for the daily management of the quality management department and the coordination of the company's internal door;9. The communication of government affairs related to quality -related government affairs, establish a good working relationship with the relevant departments of the government and drug supervision systems;10. Responsible for recruiting and expanding quality management groups in accordance with the company's development needs, and establishing the framework and development strategy of organizational members.	Under 55 years old	Doctor	1. Doctoral degree, biology, pharmacy, chemistry and other related majors, have rich work experience related to the production of biopharmaceutical production and/or quality management, including the management experience of related teams such as leadership quality control and quality assurance;2. Familiar with antibodies and/or ADC and/or reorganized protein vaccine and other biological products process processes;3. Good English listening, speaking, reading and writing ability, and proficient in computer office software;4. Careful, meticulous work, and good cross -departmental team communication skills and cooperation spirit;5. Familiar with the confirmation/verification of systems, equipment and instruments related to biopharmaceutical production, familiar with computer system verification and data electronic applications and management systems;6. Have the internationalization and commercial quality management of the biological product industry and the communication experience of foreign pharmaceutical regulatory agencies in the quality management of drugs;7. Familiar with the management specifications of the full life cycle of GMP, GLP and other drugs, familiar with the pharmaceutical government and regulations of multiple countries, and understand the development status and trend of the domestic and foreign biological products industry.	13. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
14	Major in biomedicine	Vice President of Production management	1.0	2024/12/31	1. According to the company's development strategy, organize and implement annual production plans to ensure the completion of production tasks;2. Establish and improve the production system management system and process, and strictly organize, implement, and supervise the production and operation and quality assurance of enterprises in accordance with GMP requirements;3. Responsible for the improvement of the process of processing technology in production, the transfer of new product production technology transfer;4. Responsible for managing production system safety production work, reviewing and approving the safety production rules and regulations, and supervising the implementation;5. Responsible for the management of production cost control, organize production cost accounting and analyze results;6. Participate in and lead the various certification work of GMP;7. Grasp and understand the technological development level of the same industry, and put forward the company's strategic suggestions;8. Participate in the company's major decision -making and economic activities analysis, and put forward the basis and suggestions on decision -making matters;	Under 55 years old	Master	1. Master's degree or above, medicine and biological related majors;2. Have more than eight years of large -scale sterile preparations and biopharmaceutical production quality management practice experience work experience;3. Proficient in GMP and national drug management regulations, familiar with quality assurance and quality control work; can lead the company's various types of GMP certification preparation and on -site inspection, and have the ability to lead the team to prevent and control quality risks;4. With GMP related content training experience, capable of maintaining the maintenance and management of the quality system of the enterprise, to ensure that the production and operation of the enterprise is in order;	14. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send
15	Major in biomedicine	Director of Biopharmaceutical Project Management	1.0	2024/12/31	1. Comprehensive responsibility to establish the construction of the group's biopharmaceutical project management system, including the product/project management system, specifications and standards, the formulation and improvement of the relevant process system, and supervising its implementation;2. Responsible for the management process of the new bioprisement projects before clinical, determine the project goals, formulate project plans, coordinate the work of various professional departments, ensure that the project's focus and priority level are clear, and promote it as planned;3. According to the project plan and management specifications, conduct cross -departmental project communication and coordination, supervise and inspect the project progress and quality, and make suggestions for changes if necessary;4. Responsible for monitoring the implementation process of the project, including project establishment, process, and assumptions, and timely discover and assist in solving major projects to ensure that the project is completed smoothly according to the quality, cost and time schedule of the project;5. Responsible for the measurement and analysis of project progress and quality, and issue relevant project analysis reports to relevant leaders and departments on a regular and irregular department. If necessary, make suggestions for changes;6. Responsible for formulating and implementing training programs related to project management, arrange project management candidates, and improve the overall ability of the project management team;7. Responsible for providing consulting, training and project management methods, tool application guidance and support for project management;8. Participate in and organize reports, review meetings, and summary meetings related to project management in order to improve the project management process.	Under 50 years old	Doctor	1. PhDs related to pharmacology, biology, pharmacokinetics, medicine or pharmaceutical chemistry;2. With more than 10 years of innovative drug research and development related project management experience, covering clinical pre -clinical and clinical periods, familiar with project management and phased technical transfer work, CRO company work experience or experience in large domestic and foreign pharmaceutical companies prefer;3. Has the experience of managing or guiding management at the same time (such as> 5), and more competitive development or application commercialization project management tools;4. Have a certain leadership experience with teams, team management and multi -disciplinary cross -departmental leadership;5. Have good Chinese and English expression and communication skills; can efficiently guide and promote multi -party collaboration; the ability and technical ability with strong understanding of problems, the ability to solve problems according to company leaders and collective consensus strategies, and reasonable and fast in accordance with the priority level Promote the organizational ability of the project;6. Familiar with the principles of research and guidance of new drug registration regulations at home and abroad, and pharmacological and toxicology research, and those who have experience in clinical test specifications, design and operation are preferred.	15. Provide cafeteria and staff dormitory, five insurance and one fund, supplementary medical insurance	Unlimited	Send

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