关于华领 > 招贤纳士

随着公司发展需要,我们诚挚地欢迎具有创新精神和成就事业理想的优秀人才的加入。我们将提供具有竞争力的薪酬福利待遇以及良好的培训发展机会,为每位华领员工的发展提供广阔的平台。


请将简历发送至hr@huamedicine.com

招聘职位

  • Process Chemistry R&D: Associate Director

    Job responsibility

    1. Work with internal team and external partners to create, optimize, and develop chemical process for our drug candidates.
    2. Prepare regulatory documents; Prepare and review R&D reports, tech-transfer package, patent application and other technical documents.
    3. Work with external partners (CMOs) to implement production of APIs or intermediates, and ensure on time delivery of high quality products to support Hua drug development programs.
    4. Work with external partners to implement tech-transfer.
    5. Ensure good data and knowledge management between Hua and our partners (CMOs).
    6. Help grow the talents at the external partners; Identify potential new partners and expertise in process chemistry.
    7. Serve as the expert in the area of process chemistry, contribute to internal cross function project team and buildup of CMC function.
    8. Other assigned duties to meet company objectives


    Qualifications

    • PhD in synthetic chemistry with 3-6 year experience in the field of process chemistry; oversea education or work experience in multinational companies will be a plus.
    • Solid experience in preparation of regulatory filing documents.
    • Demonstrated scientific credibility in the field of process chemistry, strong skills of problem solving.
    • Experience in working with/at CRO or CMO; and experience on plant production.
    • Good technical writing skills in both Chinese and English; Strong communication and influencing skills.
    • Extensive knowledge of general drug R&D process and knowledge of GMP production.
    • Good team player but can work independently.

  • 临床项目经理

    职位描述

    1.  全面负责项目的运行, 包括项目启动, 预算控制, 病人入组, CRF, 数据质量,以确保项目按计划完成,并符合标准流程、法规的要求和步骤。 与KOL保持良好沟通和合作关系

    2.  通过与CRO进行研究中心协同访视和日常支持,确保临床研究团队高效运作。与CRO 保持良好沟通,包括CRC, CRA, PM, DM 等

    3.  追踪并存档临床试验文档和信息, 确保完整性和准确性 

    4.  确保临床试验符合ICH-GCP及相关法规

    5.  支持协调递交至伦理委员会和法规机构的相关临床试验进展报告,并且在指定的时间内获取批件

    6.  组织相关培训以及项目电话会议

    7.  维护与试验相关的文档,数据等


    任职要求

    1.  临床医学、药理学、护理学、卫生管理或其他医学科学专业的本科学历
    2.  三至五年以上临床研究经验,丰富的临床研究相关知识和技能,以及法律法规知识
    3.  良好的英语口语和书写能力
    4.  丰富的法律法规和ICHGCP方面的知识
    5.  临床试验和法律法规的文档管理经验
    6.  良好的沟通能力

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