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医学经理

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Onsite

医学经理

RemeGen荣昌生物

医学经理

1 month ago

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Important information


Contract type:

Permanent

Location:

Beijing, China

Work mode:

Onsite

Published on:

26 September 2026

What they need


该职位来源于猎聘 Job Responsibilities:

  • Responsible for translating, proofreading, and preparing documents for international clinical trials, including the preparation of Chinese materials such as evaluation scales, study records, CRFs, informed consent forms, ethical PPTs, etc.
  • Provide medical support during the conduct of clinical trial projects, such as reviewing documents related to study, reviewing patient data, literature searches, etc.
  • Provide academic support for the global registration of company international clinical trials, such as reviewing registration documents.
  • Evaluate adverse events during the conduct of clinical trial projects and participate in discussions.
  • Complete other tasks assigned by leadership. Qualifications:
  • Master's degree or above in clinical medicine or related fields, with preference given to those with overseas study experience.
  • Proficient in English.
  • At least 2 years of experience in clinical medicine (rheumatology and immunology diseases) or working experience in large pharmaceutical companies.
  • Positive and diligent work attitude, optimistic, with affinity and teamwork spirit, good logical thinking, and analytical judgment abilities.

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