Opportunities

  • Registration Specialist

    Responsibilities:

    1. Assisting in the preparing, sorting and review of registration application materials, and submitting the registration application materials;

    2. Tracking and recording the progress of product registration;

    3. Managing registration files and other related documents;

    4. Identifying and updating product-related regulatory requirements and related standards;

    5. Completing other tasks assigned by TargetRx or superiors.

    Qualifications:

    1. Major: Chemistry, biology, pharmacy and clinical medicine related majors;

    2. Education: Bachelor degree or above;

    3. Work experience:

    ■ More than two years of relevant work experience in drug registration;

    ■ Familiar with the drug development and registration process;

    ■ Experience in R&D of small molecule new drugs is preferred;

    4. Language: Proficiency in both Chinese and English, and able to prepare registration application materials in both Chinese and English;

    5. Professional skills:

    ■ Familiar with FDA and ICH related regulations and guidelines, and search of related databases;

    ■ Familiar with international registration process;

    ■ Successful experience in clinical application is preferred;

    Other requirements: Good writing skills, strong communication skills and professional abilities.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • Patent and Government Project Application Assistant

    Responsibilities:

    1. Assisting in patent application process management, including electronic submission of patent application documents, notification download management, payment information submission, authorization registration, patent term monitoring, patent search, etc.;

    2. Keeping up-to-date of industry trends and policies of relevant ministries and commissions, and collecting valuable industry information and policy information;

    3. Collecting the application channels, information and policies of government science and technology projects, and exploring the projects that are suitable for TargetRx to apply;

    4. Assisting in the project application, including the preparing, submission and sorting of application materials;

    5. Assisting in the establishment of archives, including patent application documents and their intermediate documents, government application documents and their intermediate documents, and related contracts and disputes and other legal documents.

    Qualifications:

    1. Major: Chemistry, pharmacy and other science and engineering related majors, excellent fresh graduates are also welcomed, and the graduates with professional grades ranking top 10 are preferred;

    2. Education: Bachelor;

    3. Knowledge of patent law, CPC, CEPCT system is preferred (TargetRx provides related training in patent process management and patent law);

    4. Good team spirit, organization and execution ability and communication and coordination ability, and candidates with strong execution ability and learning ability are preferred;

    5. Certain software and hardware related knowledge, and candidates with proficiency in office software are preferred;

    6. Language: English CET-6 or above is preferred.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • New Drug R&D Information Officer

    Responsibilities:

    1. Preliminary analysis and report on the domestic and foreign development situation, market situation, patent situation, etc. of the proposed project;

    2. Researching domestic and foreign new drug R&D trends, and tracking and summarizing information on the development and registration status of various new drugs under research;

    3. Looking for potential projects for evaluation and demonstration according to TargetRx's R&D strategy through information analysis, and preparing reports;

    4. Archive management of project retrieval research materials;

    5. Assisting in R&D personnel in searching and organizing relevant technical data of the project under research;

    6. Completing other tasks arranged by superiors.

    Qualifications:

    1. Bachelor or master degree in medical chemistry, pharmacy, medicine and other organic chemistry related majors;

    2. Rich experience in new drug information collection, familiar with the R&D progress of international and domestic new drugs, familiar with patents, and familiar with new drug declaration related laws and regulations;

    3. Familiar with international and domestic major professional information websites and professional databases;

    4. Good English reading and writing skills, able to read and translate relevant documents proficiently; good writing skills, able to proficiently use OFFICE software, and strong abilities in independent learning, information collection, analysis, and summary;

    5. Carefulness and conscientiousness in work, be able to bear hardships and stand hard work, have patience, and have a sense of responsibility, and good team spirit.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • Chemistry Big Data Researcher

    Responsibilities:

    1. Building a core information database suitable for TargetRx based on TargetRx's data structure;

    2. Organizing, updating and maintaining TargetRx's drug molecule database in a timely manner;

    3. Using the knowledge of chemoinformatics to complete the bottom-level data construction and the top-level data analysis of the compound database;

    4. Overall planning of TargetRx's information system construction;

    5. Organizing chemical drug database for search and purchase;

    6. Paying attention to the research progress of chemoinformatics and the fields related to TargetRx's projects.

    Qualifications:

    1. Major: Computer science, chemoinformatics, chemistry, pharmacy;

    2. Education: Bachelor degree or above;

    3. Work experience:

    ■ One year and above;

    ■ Experience in compound database design is preferred;

    ■ Experience in pharmacy, chemistry and computer science and technology is preferred;

    4. Language: Good English reading and writing skills, and able to understand English literature in the field of medicine or chemistry;

    5. Professional skills:

    ■ Proficiency in using MySQL and other databases;

    ■ Proficiency in using Python/PHP/HTML/CSS language;

    ■ Proficiency in using Linux/Windows system;

    ■ Familiar with the use of chemoinformatics related software and data analysis tools;

    Other requirements: Good learning and logical analysis skills.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • Research Assistant in Biology

    Responsibilities:

    The main responsibilities include but are not limited to:

    1. Complete the in vitro activity test and screening of the compound according to the experimental plan;

    2. Assist to complete the communication and cooperation with various departments and related CROs;

    3. Timely write test records and reports, and conduct preliminary analysis and analysis of test results;

    4. Daily use and maintenance of related equipment in biological laboratories.

    Qualifications:

    1. Major: Biology, molecular biology, bioengineering and other related majors;

    2. Education: Master's degree;

    3. Work experience: 1-2 years of laboratory work experience (graduates are acceptable), experience in the construction of stable cell strains is preferred;

    4. Language: Excellent English reading and writing skills;

    5. Professional skills:

    ■ Familiar with biological research techniques such as cell culture and animal model construction;

    ■ Familiar with in vitro enzyme detection and in vitro cell-level activity detection methods;

    ■ Familiar with literature retrieval methods, with excellent English reading and writing skills;

    Other requirements: Good teamwork and communication skills, strong sense of responsibility, patience and carefulness, love laboratory work.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • Business Development (BD) Manager/Assistant

    Responsibilities:

    1. Following up and researching the biopharmaceutical industry; searching and reading information on the market, designated projects and technologies;

    2. Preparing medical project cooperative development documents;

    3. Assisting in the project due diligence investigation and writing the due diligence report;

    4. Contacting target cooperative companies, participating in business negotiations, establishing and expanding long-term and good strategic partnerships.

    Qualifications:

    1. Master's degree or above in pharmacy, medicine, biology, chemistry and other related majors;

    2. Work experience and project experience in well-known pharmaceutical companies and biotechnology companies are preferred;

    3. Certain understanding and tracking ability of the development of the biopharmaceutical industry; knowledge of the content of industry-related project cooperation;

    4. Good communication and negotiation skills;

    5. Good English communication and writing skills.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • Clinical Medicine VP/CMO

    Responsibilities:

    The main responsibilities include but are not limited to:

    1. Responsible for formulating new drug clinical development strategies and clinical plans, supervising and comprehensively managing the entire clinical trial process;

    2. Ensure that the clinical project is in compliance with the requirements of GCP, SOP and laws and regulations, and that the project can respond to the inspection at any time during the operation, and the requirements raised during the inspection process;

    3. Communicate with clinical medical experts, CDE review experts and other clinical research resources on clinical plan design, participate in clinical plan seminars and summary meetings, and provide relevant academic support;

    4. Manage the analysis and interpretation of clinical trial data, report clinical progress internally and foreign exchange;

    5. Conduct external academic exchanges, communicate with medical and registration regulatory agencies, industry experts, major researchers, technical partners, cooperative units (such as CRO, etc.) and other clinical related institutions;

    6. Provide effective clinical information and strategies to provide a basis for the management team to formulate the overall development strategy of the company and products;

    7. Establish a clinical research and development team, guide and train team members.

    Qualifications:

    1. Major: Clinical medicine and other medical-related majors;

    2. Education: PhD (MD/Ph.D);

    3. Work experience:

    ■ More than 10 years of clinical research and clinical trial management experience;

    ■ Successful experience in Phase 1-3 of new drug clinical trials is preferred;

    ■ Medical background are preferred;

    4. Professional skills:

    ■ Proficient in the whole process of clinical trials, familiar with the development and current status of clinical research at home and abroad; familiar with GCP and related clinical trial regulations, clinical trial requirements and procedures, and can perform related training and quality control;

    ■ Familiar with NMPA, FDA, EMA and other clinical trial regulations;

    ■ Abundant clinical trial resources (hospitals, PI, CRO, data management and statistics), good communication, organization and coordination skills and teamwork spirit;

    5. Have a professional spirit, an attitude of continuous learning, and be able to adapt to the work environment with a higher frequency of business trips;

    6. Good bilingual skills in Chinese and English.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • Senior Researcher in Organic Synthesis

    Responsibilities:

    The main responsibilities include but are not limited to:

    1. Independently completing the literature research and making a preliminary design of the route of compound synthesis;

    2. Completing the chemical reaction and conducting a comprehensive analysis of the results, and be able to complete certain difficult synthesis projects;

    3. Controlling the experimental progress of the project, guiding team members with experimental skills, and ensuring that the project is progressed and completed as planned;

    4. Writing experiment records and experiment reports clearly and completely.

    Qualifications:

    1. Major: Organic chemistry, medicinal chemistry and other related majors;

    2. Education: Master’s degree or PhD;

    3. Work experience: More than 5 years of experience in organic synthesis after obtaining master’s degree or more than 2 years of experience in organic synthesis after doctoral graduation, and the fresh doctoral/postdoctoral graduates are welcomed;

    4. Professional skills:

    ■ Proficiency in organic synthesis route design, process implementation and technical improvement;

    ■ Experience in independently completing multi-step complex organic synthesis;

    ■ Proficiency in product separation methods, spectrum analysis and structure identification;

    ■ Proficiency in searching for various documents and patents, and be able to read English documents proficiently;

    Other requirements: Strong sense of responsibility, good teamwork spirit and communication skills.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • Research Assistant in Organic Synthesis

    Responsibilities:

    1. Conducting organic synthesis experiments according to the compound synthesis design proposal;

    2. Writing test records and reports in accordance with specifications;

    3. Daily use, arrangement, cleaning and maintenance of related equipment based on the safety knowledge of synthetic laboratories.

    Qualifications:

    1. Major: Chemistry related majors;

    2. Education: Bachelor degree or above (Master's degree is preferred), more than 2 years of laboratory experience;

    3. Professional skills:

    ■ Familiar with organic synthesis, product separation and structure identification skills;

    ■ Familiar with synthesis process and pilot scale-up process and practical operation;

    ■ Familiar with literature retrieval methods, and has excellent English reading and writing skills;

    Other requirements: Good professionalism, strong sense of responsibility, rigorousness, carefulness and conscientiousness in working.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply
  • Senior Researcher in Biology

    Responsibilities:

    The main responsibilities include but are not limited to:

    1. Screening of active small molecule drugs at the enzymatic and cytological levels, and construction of related animal disease models;

    2. Pre-clinical pharmacological evaluation of small molecule drugs, including in vivo and in vitro pharmacodynamic studies, mechanism studies, etc.;

    3. Investigating new technologies and projects that meet TargetRx's development needs, and promoting project progress through cooperation with related laboratories or CROs;

    4. Timely writing test records and reports, and conduct preliminary collection and analysis of test results;

    5. Daily use and maintenance of related equipment in biological laboratories.

    Qualifications:

    1. Major: Molecular biology, cell biology, pharmacology and other related majors;

    2. Education: Master's degree or above;

    3. Work experience: More than 5 years of work experience after obtaining master’s degree or more than 2 years of work experience after doctoral graduation, and the fresh doctoral/postdoctoral graduates are welcomed;

    4. Language: Good English ability, able to read and understand English documents proficiently, and write English reports and articles;

    5. Professional skills:

    ■ Familiar with cell culture and other biological research techniques in cell biology, molecular biology, and animal model construction (experience in the construction of stable cell strains is preferred);

    ■ Familiar with in vitro enzyme detection and in vitro cell-level activity detection methods;

    ■ Experience in research on enzyme catalysis kinetics, establishment of high-throughput drug screening, and characterization and optimization of small molecule drugs;

    ■ Experience in overseas pharmaceutical/biopharmaceutical industry, preclinical bioactivity, pharmacological research, CRO management is preferred;

    Other requirements: Strong abilities in teamwork, communication, innovation, independent analysis and problem solving.

    Tips: Resume can also be sent to: hr@tjrbiosciences.com

    Apply

Company Culture

  • Our Vision

    We are confident that cancer will be cured.
  • Our Values

      T echnology
      G oal-focused
      R esiliency
    e X cellency

  • Our Mission

    To discover, develop and deliver the next generation of targeted small molecule therapies to overcome the cancer drug resistance.

    Our team is deeply committed to working relentlessly to get medicines to patients. For us, it’s not a job – it’s a personal mission.