Job description:
Cooperate with members of pharmacology and toxicology department and relevant departments to carry out screening, efficacy, action mechanism, pharmacokinetics and toxicology research related to non clinical R & D projects. Be responsible for the implementation of literature research and research, and participate in scheme design, problem solving and result analysis and interpretation;
Participate in research and inquiry on relevant research carried out by cro and cooperative institutions, communicate and coordinate the work progress of cro and cooperative institutions and solutions to problems; Complete other tasks assigned by the company.
Write non clinical research related documents and reports;
Write non clinical pharmacological and toxicological data, and cooperate with department members and relevant departments of the company to complete ind or listing registration application, or relevant IP application;
Participate in project initiation and put forward opinions or suggestions;
Participate in the company's professional evaluation of due diligence or investment projects.
Job requirements:
Master degree or above with good background knowledge in pharmacology, pharmacokinetics, toxicology or related disciplines. Working experience in non clinical pharmacology, toxicology or clinical pharmacology is preferred;
Master the experimental methods related to pharmacology, pharmacokinetics or toxicology, and be able to participate in the construction of in vitro and in vivo drug screening model, activity screening, pharmacokinetics and pharmacodynamics evaluation of new drugs through cro;
Have certain project management experience, clear working ideas, and have certain ability to analyze and solve problems;
Strong Chinese writing ability, understand the registration and patent application process of new drugs;
Good communication skills and teamwork spirit, strong sense of responsibility and proactive spirit.

Job description:
1. Be responsible for in vitro and in vivo efficacy, DMPK and toxicological safety assessment tests and preclinical development tests of new drug R & D projects, including literature research, formulation and implementation of test scheme, sorting and analysis of test results;
2. Investigate and inquire about the relevant research carried out by cro and scientific research institutions, and communicate and coordinate the work progress of cooperative units and entrusted units;
3. Be responsible for the preparation of preclinical pharmacological and toxicological declaration materials, and cooperate with registration to complete ind and NDA declaration;
4. Participate in project initiation and put forward opinions or suggestions from a professional perspective;
5. Participate in the company's professional evaluation of due diligence or investment projects.
Job requirements:
1. Pharmacology, pharmacokinetics, ADMET and other related majors and knowledge. The post of senior researcher requires a doctor's degree, and the post of researcher requires a master's degree. Experience in preclinical pharmacology, toxicology and clinical pharmacology evaluation of new drugs is preferred;
2. familiar with the relevant experimental methods of pharmacology and toxicology, and be able to independently undertake or through cro to construct and select the screening model of drugs in and out of and out of the body, and to evaluate the pharmacodynamics and pharmacodynamics;
3. Have certain project management experience, clear working ideas, and strong ability to analyze and solve problems;
4. Strong writing ability, familiar with new drug registration and patent application process;
5. Good communication skills, teamwork spirit and strong sense of responsibility.

Job description:
1. Assist the superior leaders in selecting, managing and coordinating the research center and third-party partners (including cro, SMO, central laboratory, data management and statistical analysis, cold chain transportation, etc.) to ensure that the services are provided according to the contract requirements;
2. Follow up the clinical trials of the company's products through the standardized supervision process, and carry out them in strict accordance with the requirements of national laws and regulations and the established clinical trial scheme;
3. According to the actual needs of the trial scheme, participate in the screening, project start-up, ethical review, process supervision, center closure, etc. of the clinical research center;
4. Timely and effectively collect relevant clinical research data, ensure that all necessary documents are updated and complete in time, and ensure that all clinical trial data are true, accurate and complete;
5. Timely report and summarize the progress of clinical trial, and assist in solving the problems in the process of clinical trial;
6. Complete the contract signing, payment, drug application and inventory, coordination of sample delivery and other processes related to clinical trial activities;
7. Coordinate and maintain a good cooperative relationship with clinical trial units to ensure the smooth completion of clinical trials;
8. Complete other tasks assigned by superior leaders.
Qualification
1. Bachelor degree or above in medicine or pharmacy;
2. More than 1 year of CRA, CRC or other relevant experience in pharmaceutical enterprises and cro companies is preferred;
3. Be familiar with the whole process of clinical trial and relevant regulations and policy requirements, GCP certificate is preferred;
4. Have a certain foundation in clinical medicine and pharmacy, be familiar with the operation process of clinical trials, and understand relevant laws and regulations;
5. CET-4 or above, good reading and writing skills;
6. Strong organization, coordination and communication skills and pressure resistance;
7. Strong learning ability, quickly familiar with and master new projects and new regulations;
8. Be able to travel irregularly due to work needs.

Job description:
1. Be responsible for the selection of clinical research cooperation units, including clinical research center, cro company, insurance company, transportation company, testing unit, etc;
2. Be responsible for managing cro and other relevant units to ensure that the project operates as planned;
3. Be responsible for the budget and progress control of the project;
4. Be responsible for internal and external communication and coordination to ensure the progress and quality of clinical research;
5. Be responsible for GCP, operation training, etc. for relevant personnel of the project.
Qualifications:
1. Major in medicine and pharmacy;
2. At least 2 years of clinical trial project management experience, with innovative drug clinical research project management experience is preferred;
3. GCP and guiding principles of relevant national laws and regulations on clinical research, organization and implementation of clinical trials, medical professional knowledge and information analysis ability;
4. Have good planning ability, organization and coordination ability and communication ability;
5. Be able to travel.

Job responsibilities:
1. Preparation of application materials for registration of innovative drugs;
2. Design and writing of clinical research schemes for each phase;
3. Design and writing of medical materials required for clinical research;
4. Program training for relevant personnel of the project;
5. Medical supervision during the operation of clinical research projects;
6. Review relevant medical documents of cro company, including ethics submission materials, summary reports, etc;
7. Maintenance of clinical experts.
Job requirements:
1. About 5 years working experience in clinical medicine, biology and related majors, master's degree or above;
2. Experience in comprehensive project management or innovative drug development is preferred;
3. Be good at literature retrieval and information analysis;
4. Excellent communication, coordination and execution skills, and excellent team spirit.