Job Responsibilities:
1. Responsible for the management of clinical research data and service providers, provide professional support for data management for the company's clinical trial projects, and formulate clinical research data management solutions and schedules.
2. Responsible for CRF design or review, responsible for database review, and promote database launch.
3. Participate in writing or reviewing data management related documents of external suppliers, such as DMP, DVP, DMR, etc.
4. During the project execution process, timely conduct data verification, database QC, questioning review and other work.
5. Formulate and implement database construction and data management related SOP.

Job Requirements:
1. Bachelor degree or above in statistics, epidemiology, medicine, computer and other related majors.
2. More than 2 years of clinical trial data management experience.
3. Familiar with more than one database configuration and can independently write verification procedures.
4. Familiar with the various regulations and guidelines for data management and statistical analysis of ICH and CFDA, familiar with the process of data management, and familiar with CDISC standards.

Job Responsibilities:
1. Preliminary writing and review of clinical trial medical documents.
2. Assist in clinical operation and medical communication, organize medical literature, collect and organize medical data, and conduct preliminary data analysis.

3. Assist in medical monitoring.

Job Requirements:
1. Master's degree or above, major in clinical medicine.
2. More than 1 year of clinical work experience, proficient in office, drawing and other scientific research software.
3. Those who have participated in the writing of medical documents for clinical trials are preferred.

Job Responsibilities:
1. Responsible for the preliminary evaluation experiments of molecular biology and in vitro cell-level drugs, such as cell experiments, animal experiments, biochemistry and molecular biology experiments.
2. Able to work independently under the guidance of the project leader and complete the R&D report independently as required.
3. Priority is given to those with AAV R&D experience, those who are good at cell culture or animal experiments, and those who have experience in qPCR, Western Blot, and Elisa.

4. Complete other tasks assigned by the person in charge.

Job Requirements:
1. Fresh graduate or above, graduated in cell biology, molecular biology, virology, immunology, pharmaceutical related majors or graduation thesis related to molecular biology and/or cell biology technology.
2. Have a solid theoretical foundation in molecular biology and cell biology, and be proficient in basic experimental techniques in molecular biology and/or cell biology, including molecular cloning, cell culture, real-time PCR, ELISA, Western Blot, fluorescence microscopy and other related technologies.
3. Have strong English reading ability, and be able to effectively search and understand relevant English literature; 4. Work diligently, be proactive, motivated, and be able to cooperate and communicate with colleagues.

Job Responsibilities:
1. Effectively promote and implement the internal and external process work of registration affairs, assist in the management of registration projects, and follow up the progress of project implementation.
2. Responsible for the collection and compilation of data in the process of registration management, and the compilation of various information resources within the department.
3. Assist the communication and coordination between this department and other departments, and do a good job in the management of documents and the uploading and issuing of document information.
4. Assist in the relevant work of department system construction.
5. Query, organize and analyze laws and regulations, and the latest dynamic information.
6. Responsible for the daily affairs of the department, meeting support, and the organization and follow-up of meeting minutes.

7. Complete other work arranged by the company leaders and department heads.

Job Requirements:
1. Bachelor degree or above, no major limit.
2. Proficient in using office software and good document processing skills.
3. Optimistic, cheerful and motivated, good communication skills and coordination skills, and able to withstand high-intensity work pressure.
4. Strong execution ability, rigorous work attitude, carefulness, and strong sense of responsibility.
5. Strong writing skills, strong learning ability, and good logical thinking.

Job Responsibilities:
1. Familiar with virus purification production operations, including assisting in the optimization of purification processes, and responsible for the production work of the downstream purification section according to the process regulations; such as: solution preparation, virus filtration, ultrafiltration, etc.
2. Participate in GMP training and follow GMP and process requirements for production operations, and be responsible for the operation of the purification system in accordance with GMP requirements.
3. Fill in production records and organize experimental data reports as required, summarize the data of the purification process operation process in a timely manner, and report abnormal situations in a timely manner.
4. Responsible for the daily operation, management, cleaning, maintenance and verification of post equipment, and participate in the maintenance and management of other instruments in the workshop.
5. Accept and complete other tasks assigned by superiors on time.

Job Requirements:

1. Biology, chemistry, pharmacy, pharmaceutical and other related majors; bachelor degree or above; (fresh graduates are acceptable).
2. Understand the work content related to cell culture and be familiar with bioreactor operation.
3. Familiar with GMP regulations, experience in GMP and cell culture work is preferred.

Job Responsibilities:
1. Participate in the development and verification of new methods for gene therapy drug quality research.
2. Participate in gene therapy R&D project research.
3. Participate in the discussion, design and determination of experimental plans.
4. Responsible for the implementation of specific experiments, such as biochemical, molecular, cell and other experimental operations.
5. Responsible for the recording, summary, analysis and report writing of experimental raw data.
6. Actively learn and master the principles and operating skills of various experiments in this department, as well as the use of instruments and equipment.
7. Actively learn new experimental skills and develop new analytical methods.

8. Take responsibility for part of the laboratory management and daily maintenance of instruments and equipment.

Job Requirements:
1. Bachelor degree or above in medicine, biology, pharmacy, chemistry and other related majors.
2. Have a strong sense of professionalism and responsibility, be proactive and down-to-earth.
3. Have a strong team spirit, good interpersonal communication skills, and meticulous and patient qualities.
4. Love laboratory work, have strong hands-on and learning abilities, and are willing to explore new experimental techniques.
5. Have a certain level of Chinese and English reading and writing skills.