Responsible for pre-clinical research and development project research, planning and implementation, setting goals and budgets, organizing and implementing project progress, and implementing quality controlCoordinate research progress, review relevant data, ensure project completion on schedule and quality, organize and coordinate R&D cooperation projects with universities and other scientific research institutionsCoordinate and cooperate with other R&D departments to promote the overall drug development process, and formulate the annual product development plan within the framework of the company's product development strategic directionReview the pharmacology, efficacy, pharmacokinetics and toxicology programs and reports of preclinical projects, and be responsible for the company's Chinese medicine refined pieces. New product research and development of traditional Chinese medicine preparations and related project managementCooperate with or be responsible for the preparation and arrangement of drug registration materials, and communicate with relevant registration departments at home and abroadCollect and master dynamic information such as policies, regulations and technical requirements

Assisted in drug research and development projects, independently designed and guided drug preparation research, including literature research. Prescription design. Process research. Stability research. Process amplificationAssisted the project research and development plan and coordinated the implementation of the plan, analyzed and timely solved the problems arising from the research and developmentResponsible for solving technical difficulties and related problems of the project and cross-departmental communication, able to effectively realize the transformation of pharmaceutical technology from small laboratory trials to pilot trials and industrializationIndependently write or assist in writing relevant drug application materials according to the requirements of drug registration regulations. Original recordResponsible for the professional research and development of preparations, and prescription screening. Process research and optimization, transform the pilot test and mass production of the developed preparation and write the application data. Original records. Ensure the standardization of R&D projects. Authenticity and integrity

Identification and analysis of active substances in the early stage. For example, XX pharmaceutical company involved in the project is engaged in the extraction and identification of natural products of Chinese medicinal materials, with the purpose of helping pharmaceutical companies to find active ingredients that can be applied in drug research and development.In the middle stage, the research and development of finished drugs, including chemical drugs, vaccine drugs, genetic engineering drugs and other research and development of different drugs, as well as the technology research and development of drug preparations, pharmacotoxicity analysis, pharmaceutical process improvement and other important links.There are many types of work in the late design, most of which are auxiliary and supportive work, such as research on the clinical application of finished drugs, preparation of materials for new drug approval or patent application, etc.In addition to having excellent professional and technical background, the corresponding management personnel of these works also need to make overall planning and task deployment for the project or department work, and assume the responsibilities of team management.

Responsible for pre-clinical research and development project research, formulation of implementation plan, target budget and quality control regulationsCoordinate research progress with pharmaceutical project partner units and R&D department, review relevant data, write analysis report, guarantee development processCooperate with pharmacology and Toxicology department to review pharmacology, efficacy, pharmacokinetics and toxicology protocols and reports for preclinical programsWrite and organize drug registration data, and communicate with domestic and foreign drug registration departmentsCollect information on serious adverse events and adverse reactions to ensure drug compliance with pharmacovigilance regulationsMaster the policy, regulations and technical requirements of preclinical research of new drugs

Mainly engaged in the establishment of drug quality analysis methods and method verification Completed instrument analysis and atlas analysis according to the experimental schemeAssisted in sorting out experimental data and proofreading dataUnder the guidance of the superior, responsible for the quality research work of the project, such as drafting the research plan, promoting the research plan and solving the problems, writing and reviewing the research report, etc.