1. Implement pre-filing preparations and post-filing prosecutions in the technical area of pharmaceuticals, including prior art search, patentability analysis, drafting, and office action response;

2. Implement patent monitoring;

3. Implement patent reexamination and invalidation.

1. Master or above in a relevant discipline such as pharmaceutical, chemistry or related field;

2. Have pass the patent attorney qualification exam in China with 1+ year of relevant work experience in patent drafting;

3. Have excellent English skills (equal or above CET 6 level);

4. Have a strong sense of professionalism, responsibility, and team spirit; Have strong logical thinking and communication and coordination skills.

1. Manage the process of patent case, double-check the time limit, monitor the progress;

2. Review of relevant intellectual property terms in agreements/contracts;

3. Drafting or review of agreements/contracts in patent licensing and technology transferring;

4. Search and analyze materials related intellectual property, such as publications, laws, cases etc.

1. Bachelor degree or above, major in law, intellectual property is preferred;

2. 1+ year of work experience in a law firm;

3. Familiar with relevant laws and regulations in the field of intellectual property such as patent and trade secret;

4. Have excellent English skills (equal or above CET 6 level);

5. Proficiency in software including PowerPoint, Word, Excel etc;

6. Have a strong sense of professionalism, responsibility, and team spirit; Have strong logical thinking and communication and coordination skills.

1. Responsible for the project management of early projects, including but not limited to: project/target research, promotion of drug target screening (molecular biology, cellular and animal screening), lead compound screening, and druggability evaluation;

2. Assist in the formulation of new drug preclinical research plan, program design, organization and implementation, process control, result summary and analysis summary;

3. Complete communication and cooperation with various departments and related CROs to promote project progress;

4. Complete the tracking of the progress of various research work to ensure the progress of the project; organize the project process files and file them regularly;

5. Participate in the compilation and collection of PCC data, the compilation, review, and submission of IND application data;

6. Assist the intellectual property department to complete the drafting of patent materials and provide technical support;

7. Complete other tasks arranged by the company or superiors.

1. Majors in medicinal chemistry, biology, pharmacology, and pharmacokinetics;

2. Master's degree or above (received fresh doctoral students);

3. Experience in small molecule new drug development and project management is preferred; familiar with drug development and application process, and have a certain understanding of pharmacology, pharmacokinetics, and toxicology; working experience in pharmaceutical companies or CRO is preferred; CRO Management experience is preferred;

4. Have good Chinese and English skills, and can perform the task of writing and reviewing registration application materials in both Chinese and English;

5. Have a sound basic training in scientific research, have experience in the research and development of new small molecule drugs, and be familiar with project management knowledge, processes, and methods;

6. Understand the pre-clinical research and development process of drugs; understand the regulations, guiding principles of NMPA and FDA, and the content and process of registration application;

7. The work is rigorous and serious, with R&D thinking, good teamwork ability, communication ability, emergency ability and problem-solving ability.

1. Establish and maintain the management of clinical research-related documents and archives, establish, and maintain the update management of the project folder, to track the compliance of the research center, and operate at the specified time of the project;

2. Assist the clinical research team in the preparation, processing, distribution, filing and archiving of clinical research documents and reports according to the scope of work and standard operating procedures. Assist in regular checking of the accuracy and completeness of research documents;

3. According to the project requirements, assist the project manager in clinical trial material management, expense management, milestone event management, progress and quality management, data cleaning, on-site inspection, etc.

1. Bachelor degree or above; major in medicine or pharmacy (or equivalent training and experience);

2. 3+ years of relevant work experience in clinical trial monitoring or management;

3. Familiar with ICH-GCP, NMPA GCP and related regulations;

4. Familiar with the operation procedures of different departments of clinical trials;

5. Effective written and oral communication skills, good English written and oral skills;

6. Good computer skills including Word, Excel, PowerPoint.

1. Establish the company's clinical quality management system and maintain normal operation;

2. Responsible for implementing various quality management rules and regulations within each department of the clinical system, and conducting audits and inspections of suppliers, CRO companies, commissioned inspection laboratories, clinical trial centers and other cooperative units/institutions involved in clinical work according to quality management requirements. , to ensure that clinical trial activities carried out in suppliers, CRO companies, commissioned inspection laboratories, clinical trial centers and other cooperative units/institutions comply with GCP regulations and the company's various quality management rules and regulations;

3. Establish the company's GCP document management system, standardize the drafting, revision, review, approval, and entry into force of documents, and ensure that each department's activities related to clinical trials have SOP guidance that meets regulatory requirements, records and compliance with regulations archiving;

4. Responsible for organizing the formulation of training management documents in the GCP system, establishing a GCP training system, and supervising various departments to complete the training work of their own departments as required;

5. Responsible for organizing and implementing the inspection and auditing of the clinical trial process, training and guiding each clinical QC to carry out quality management in all aspects of the clinical trial process;

6. Responsible for establishing and improving various quality management processes, including but not limited to change management process, deviation handling process, audit process, CAPA process, risk assessment process, etc., and ensure that each department cooperates with the quality control department to carry out quality management work according to the process;

7. Responsible for establishing a supplier management system, organizing the formulation of relevant documents and records for supplier management, and carrying out supplier management work as required.

1. Have a medical-related college degree or above and more than 5 years of clinical quality management work experience, and be able to independently lead the clinical QC department to carry out work;

2. Be proficient in relevant laws and regulations of the clinical work industry, master GCP professional knowledge, be familiar with the clinical trial process and various processes of clinical trial quality management, and be able to find and solve quality-related problems in a timely and effective manner;

3. Successful experience in the establishment of clinical quality management system, clinical project application and inspection, and successful experience in multinational clinical project application and inspection is preferred;

4. Possess certain forward-looking and foresight, and can put forward plans for potential risks in advance;

5. Have excellent coordination and communication skills, recognize the company's corporate culture, be diligent and dedicated, have excellent professional ethics and teamwork spirit.

1. Conduct the literature research independently, and make the rough synthetic route design of target molecules;

2. Conduct synthetic experiments and analysis of the results, and be able to handle difficult projects;

3. Monitor the experimental progress of projects, and Keep the projects on Schedule by providing experimental skills guidance to team members;

4. Write experimental records and reports detailed and clearly.

1. Major in organic chemistry, medicinal chemistry or other directly related field;

2. Master's degree or above;

3. 5 years or above (with MS); 2 years or above(with PhD); Fresh PhD/Postdoc is acceptable;

4. Proficiency in organic synthetic route design, organic process, and technical improvement;

5. Experienced in multi-steps synthesis of complex molecules;

6. Skilled in isolation, purification, chromatographic analysis, and structural identification;

7. Proficiency in retrieval of literature and patents, and reading English paper.

1. Conduct organic experiments, according to designed synthetic route protocols;

2. Maintain detailed records of experiments and outcomes in accordance with the standard;

3. Strong knowledge of lab safety, and equipment daily use, arrangement, clean-up, and maintenance.

1. Major in organic chemistry, medicinal chemistry or other directly related field;

2. Bachelor's degree or above;

3. Practical experience in lab (1-2 years);

4. Familiar with organic synthesis, purifications, and structure identification;

5. Familiar with synthesis process, scale-up and practical operation;

6. Familiar with literature search, and good English reading and writing skills.

1. Responsible for the drug activity screening of small molecule drugs at the enzymatic and cytological levels;

2. Preclinical pharmacological evaluation of small molecule drugs, including in vitro and in vivo pharmacodynamic and mechanism of action studies;

3. Investigate the relevant literature and new technologies of the research project, and promote the progress of the project in a timely manner;

4. Write test records and reports in a timely manner, and conduct preliminary sorting and analysis of test results;

5. Daily use and maintenance of biological laboratory related equipment.

1. Major in molecular biology, cell biology, pharmacology, and other related field;

2. Master's degree or above;

3. 5 years or above (with MS); 2 years or above(with PhD); Fresh PhD/Postdoc is acceptable;

4. Experience in immunology, structural biology, or stable monoclonal cell construction is preferred;

5. Rich experience in cell culture;

6. Experience in enzymatic kinetics research, establishment of high-throughput drug screening and small molecule drug characterization and optimization;

7. Experience in overseas pharmaceutical/biopharmaceutical industry, preclinical biological activity, pharmacological research, and CRO management is preferred;

8. Good English ability, proficient in reading and understanding English literature, writing English reports and articles;

7. Strong teamwork, communication, innovation and independent analysis and problem-solving skills.