| CRA | 1. Responsible for the development, promotion, daily inspection and quality management of research center projects; 2. Responsible for the relationship maintenance at the basic level of the research center; 3. Completed and fed back all reports that the company needed to collect; 4. Completed other tasks assigned by superior leaders. | 1.Bachelor degree or above in medicine or related major, CET-4 or above; More than 1 year of clinical supervision experience, tumor project experience is preferred; 3. Familiar with GCP, ICH-GCP and relevant regulations, laws and regulations of clinical research; 4. Adapt to business trip; 5. Good communication skills, executive ability, perception and interpersonal skills; 6. Proficient in using various office software. |
| PM | 1. Managed the pre-market clinical trials of the company's new products under the leadership of the medical person in charge, controlled the overall quality of clinical implementation, and ensured that the project complied with relevant national regulations and requirements; 2. Manage the overall process control of clinical trial project implementation to ensure that the project schedule meets the requirements of THE R&D plan; 3. Communicated with researchers about relevant issues of the experiment to ensure the progress of the experiment; 4. Completed other tasks assigned by superior leaders. | 1, Major in Medicine, clinical, health or related, bachelor degree or above; 2. Premarket drug clinical trial experience is preferred, medical device clinical trial experience is preferred; 3. Good communication, strain ability and problem solving ability; 4. Adapt to business trips. |
| Medical Manager | 1. Under the leadership of medical leaders, collect and organize the data of clinical research projects, draft or revise the clinical trial protocol, investigator's manual, safety update report, informed consent, clinical summary report and other trial related documents; 2. Guided the development or revision of the department's medical data, wrote SOP for related operations, and trained related personnel; 3. Regularly collecte and sorte out serious adverse events or unexpected adverse events occurred during clinical trials, tracke and collect the information of adverse reactions of relevant drugs at home and abroad, and communicate and discusse with the project team and researchers; 4. Evaluate and communicate the clinical application and medical practice of new varieties to be introduced and developed by the company; 5. Keep track of medical advances in related fields. | 1. Master degree or above in medicine or pharmacy; Major in hematology or hospital experience is preferred; / Bachelor degree or above in Medicine, Pharmacy, Preventive Medicine, Animal Medicine or other medical related majors; Major in hematology or hospital experience is preferred; 2. Premarket drug clinical trial experience is preferred, medical device clinical trial experience is preferred; 3. Good communication, strain ability and problem solving ability; 4. Adapt to business trips; 5. Good English listening, reading and writing skills. |
| Formulation Development Researcher | 1. Responsible for the development of preparation prescription for each project; 2. Assist in the development of antibody purification process and coupling process; 3. Write the relevant application materials of preparation prescription; 4. Operate related instruments and carry out daily maintenance. | 1. Bachelor degree or above in chemistry, biology, pharmacy or related; 2. Familiar with the formulation process development process, familiar with the principle and operation of DSF, DSC and other instruments, and able to effectively analyze the data; 3. Proficient in reading English literature, strong ability to consult Chinese and English literature; 4. Conscientious, responsible, practical, diligent, diligent, with good team spirit; |
| Researcher of Drug Freeze-Drying Process | 1. Able to independently complete the selection and design of the formulation of chemical drug development, and independently carry out and complete the experimental work; 2. Familiar with HPLC, UPLC operation process and chemical lyophilization process development process; 3. Responsible for writing the preparation part of the application data, and sorting out the original records and reports; 4. Understand the approval requirements of chemical drugs and relevant laws and regulations. | 1. Major in pharmacy, pharmaceutical preparation, biology, etc., bachelor degree is required with more than two years working experience in related enterprises, master degree is preferred; 2. Familiar with drug research and development process, master professional knowledge of drug preparation research and development, quality analysis, workshop production and other aspects, and be skilled in operation of drug preparation research and development equipment; 3. Strong experimental skills and theoretical knowledge of pharmaceutical preparations, able to carry out process research independently; 4. Proactive, rigorous, efficient, responsible, good team spirit, good at learning and accepting new knowledge and skills. |
| Pharmaceutical Chemistry Synthesis Researcher | 1. Able to skillfully complete a variety of chemical reactions; Independently designed and performed multi-step organic synthesis; 2. Proficient in literature review and atlas analysis. 3. Able to find and solve problems in the experiment; 4. Good experimental operation ability, good experimental skills. | 1. Bachelor degree or above in organic chemistry or pharmaceutical chemistry, with strong interest in new drug development; 2. Solid knowledge of organic and pharmaceutical chemistry; 3. Serious and positive in work, strong sense of responsibility and enterprise; 4. Good team spirit; 5. Good English writing ability, good work summary and report ability. |
