• Work Pace Position Education Work Experience Number of recruits Salary Operate
  • Nanjing QC specialist / Manager Undergraduate / / Face to face discussion
    Job Requirements

    1. Assist in sorting out the management information of the quality control department;

    2. Carry out on-site quality control and RBM quality control according to the quality control plan;

    3. Supervise and urge the joint supervision of all project teams;

    4. Follow up the rectification and solution of relevant problems after joint supervision , institutional quality control and external quality control of all project teams ;

    5. Other affairs of quality control department


    Post Requirements

    1. Pharmaceutical, medical or related professional background, bachelor degree or above

    2. Two years of excellent CRA experience can also be considered, and device project experience is preferred

    3. Professional skills: strong learning ability, communication and coordination ability, analysis ability and team writing ability

    4. Quality requirements: good health, good image and good temperament.


  • Nanjing Clinical Trial Assistant Undergraduate More than two years 2 Face to face discussion
    Job Requirements

    1. Assist PM and CRA to manage trial related documents, such as collection, scanning, copying, archiving and maintenance of clinical trial research data;

    2. Cooperate with PM to collect the information of research institutions from CRAs and update the project management tracker;

    3. Assist in the management of test materials, and complete the distribution, recovery and destruction of project materials after the approval of the project manager;

    4. Coordination of clinical trial related meetings and training, such as arrangement and recording of research meetings;

    5. Other support work for CRA team.


    Post Requirements

    1. Bachelor degree or above in medicine and health and other related majors;

    2. Be familiar with the application of word, Excel and other office software;

    3. Good Chinese expression skills, able to sort out basic English documents;

    4. Have a certain understanding of clinical trials and relevant laws and regulations of domestic clinical trials;

    5. Have basic communication skills, strong sense of responsibility, hard-working and willing to learn;


  • Nanjing Clinical Research Associate Undergraduate More than three years 2 Face to face discussion
    Job Requirements

    1. Implement the supervision of the clinical research center in charge according to the supervision plan;

    2. Ensure that the clinical trials of the research center are carried out in strict accordance with the protocol, GCP and relevant laws and regulations, and protect the rights and interests of subjects;

    3. Assist researchers in solving possible problems during the experiment;

    4. Ensure that the research data are recorded in the case report in a timely, accurate and complete manner;

    5. Collect, sort out and archive the research documents according to SOP;

    6. Be able to undertake the work of project assistant and assist the project manager in quality control of clinical research;

    7. Complete other related work assigned by PM manager.


    Post Requirements

    1. Bachelor degree or above, major in medicine or related life sciences;

    2. Have strong team spirit, communication and problem-solving ability, and be able to business travel;

    3. Those who have participated in formal GCP training are preferred.


  • Nanjing Intern Undergraduate Unlimited 5 Face to face discussion
    Job Requirements

    1. Assist the project manager and clinical experts to complete the design of research scheme and other test data;

    2. Be responsible for the investigation, screening, coordination, ethics review, agreement signing, supervision and quality control, recruitment progress supervision, follow-up and conclusion of clinical trial institutions;

    3. Coordinate researchers, management institutions, CRC, sponsors, etc., and manage clinical trial affairs;

    4. Data recovery and query resolution, assist in data management and statistical analysis;

    5. Write the summary of the center and sign and seal the clinical trial documents;

    6. During the training period with immature CRA skills, you need to work as a clinical research assistant (CTA)


    Post Requirements

    1. Full time bachelor degree or above, major in medicine or related life sciences, fresh graduates or students without course tasks.

    2. Be interested and enthusiastic in the clinical trial industry;

    3. Understand relevant laws and regulations of clinical trials;

    4. Those who have participated in formal GCP training are preferred;

    5. Excellent academic performance and good English level;

    6. Strong communication, understanding, analysis, induction, coordination, persuasion, organization and team spirit.