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  • secretary of the board administration section Guangzhou - huangpu district
    Apply immediately
    workplace:Guangzhou - huangpu district
    department:administration section
    education:Bachelor or above
    numbers:1 person
    responsibilities:
    1. Summarized product requirements through data collection, peer research and communication with clinical experts, and participated in the daily development process of r&d;
    2. Organize clinical trials, statistical analysis of data, and write and publish articles;
    3. Responsible for the company's internal and external clinical knowledge and equipment clinical knowledge training, clinical academic support;
    4. Assist product registration to write clinical trial plans, organize and supervise clinical trials, and write clinical trial reports;
    5. Assist in sorting out and exporting clinical marketing materials.
    job requirements:
    1. Master degree or above in biomedical engineering or clinical medicine, with solid basic medical knowledge, experience as a clinician is preferred;
    2. Rich clinical knowledge, familiar with clinical business and hospital process, and familiar with clinical verification process of medical devices;
    3. Master SPSS and other statistical methods, have good ability to search, read and write medical documents, and write medical papers; First author in core journal is preferred;
    4. Good organization and coordination ability and team spirit;
    5. Honest and trustworthy, with good professional ethics, good sense of service and dedication;
    6. Good language expression, good communication skills, good writing skills, cet-4 or above.
  • engineer R&D division Guangzhou - tianhe district
    Apply immediately
    workplace:Guangzhou - tianhe district
    department:R&D division
    education:Bachelor or above
    numbers:1 person
    responsibilities:
    1. Summarized product requirements through data collection, peer research and communication with clinical experts, and participated in the daily development process of r&d;
    2. Organize clinical trials, statistical analysis of data, and write and publish articles;
    3. Responsible for the company's internal and external clinical knowledge and equipment clinical knowledge training, clinical academic support;
    4. Assist product registration to write clinical trial plans, organize and supervise clinical trials, and write clinical trial reports;
    5. Assist in sorting out and exporting clinical marketing materials.
    job requirements:
    1. Master degree or above in biomedical engineering or clinical medicine, with solid basic medical knowledge, experience as a clinician is preferred;
    2. Rich clinical knowledge, familiar with clinical business and hospital process, and familiar with clinical verification process of medical devices;
    3. Master SPSS and other statistical methods, have good ability to search, read and write medical documents, and write medical papers; First author in core journal is preferred;
    4. Good organization and coordination ability and team spirit;
    5. Honest and trustworthy, with good professional ethics, good sense of service and dedication;
    6. Good language expression, good communication skills, good writing skills, cet-4 or above.
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