Social Responsibility

We have been making unremitting efforts to actively introduce the cutting-edge innovative medicines and therapeutic solutions for the improvement of the public health

Work together with the government, health agencies, non-profit organizations and other communities, Antengene aims to promote charity and benefit more patients

Social Responsibility

We have been making unremitting efforts to actively introduce the cutting-edge innovative medicines and therapeutic solutions for the improvement of the public health

Work together with the government, health agencies, non-profit organizations and other communities, Antengene aims to promote charity and benefit more patients

Antengene is a member of US-China Anti-Cancer Society. Since the registration, we have been actively involved in the topics of anti-cancer publicity, popularization of oncology scientific treatment and other activities.

Antengene also participated the donation program launched by the Association of Leukemia and Lymphoma in the United States.

Working at Antengene

At Antengene, our greatest assets are our people. We work together across the world with the most talented experts and the most innovative pharma and biotech companies to bring cutting-edge treatment solutions to China and other Asian markets.

As a team, we dream big and aim high. As a company, we strive for excellence in our work to deliver transformative medicines and to help improve the lives of patients and their families.

If you are passionate about the life science industry, have an entrepreneurial spirit and have been looking for an opportunity to make a real impact, join us at Antengene!

All interested talents are welcome to send your resume and/or CV to recruitment@antengene.com.

Job Vacancy

  1. Medical Advisor

    Scientific Affairs / Shanghai/Beijing

    Responsibilities:

    Establish Medical Strategy for pre-launch brand and pipeline products.

    Conduct productive engagement with key national stakeholders.

    Design and compose study protocol post launch.

    Design and implement medical activities.

    Provide strategic advice and support for corporate business development.

     
    Qualifications:

    Master degree or above in Clinical Medicine/Biology.

    3Y+ medical experience on Hematology/Solid Tumor area.

    Experience of clinical trial design and implementation.

  2. Clinical Project Manager

    Clinical Operations / Shanghai

    Responsibilities:

    Be responsible for study protocols, CRF, ICF, lab manual, pharmacy manual, clinical monitoring plan.

    Keep closely relationship with site and submissions for ICH-GCP, site contract process and governor approval.

    Contribute to PI and site identification, communications, and initiation.

    Contribute to site feasibility process.

     

    Qualifications:

    Bachelor degree or above in Clinical Medicine/Pharmacy.

    1Y+ clinical project management, oncology project experience preferred.

    International project experience is preferred.

  3. Study Physician

    Clinical Development / Shanghai/Beijing

    Responsibilities:

    Manage global or regional studies and involve in the design, conduct, monitoring, data interpretation and reporting of individual clinical trials.

    Provide expert scientific and clinical input to Clinical Development, Regulatory Affairs, Biostatistics, Data Management, and other related departments.

    As a trial level physician and medical monitor for clinical studies.

     

    Qualifications:

    M.D. degree, 2Y+ industry drug development experience.

    Experience specific to oncology preferred.

    Fluent in English, both verbal and written.

  4. Safety Physician

    Clinical Development / Shanghai

    Responsibilities:

    Perform Medical Review of adverse event reports including but not limited to all serious, events of special interest.

    Provide input to key internal safety documents, including Risk Management documents (RMPs), development and updates/maintenance of expectedness guides.

    Provide support for investigator brochures, protocols, informed consents, final study reports, as appropriate.

     

    Qualification:

    M.D. degree & 5Y+ pharmacovigilance experience in drug development pharma/biotech industry.

    Experience specific to hematology preferred.

    Fluent in English, both verbal and written.

  5. Medical Writer (Senior)

    Clinical Development / Shanghai

    Responsibilities:

    Research, write, and edit clinical documents, including clinical study protocols, clinical study reports, IB, ICF, RMP, clinical plan outlines, and scientific manuscripts.

    Review statistical analysis plans and mock statistical output to assist in determining appropriateness of content/format for clinical writing.

    Provide medical editing review of draft and final documents.

    Perform literature searching and reviews as necessary.

     

    Qualification:

    Medical related degree & 2Y+ medical writing experience.

    Experience in clinical study design and protocol development and CSR/writing.

    Fluent in English, both verbal and written.