• 招聘类型：社招
• 工作性质：全职

职位描述

Mission/Purpose of Position：Provide scientific support including clinical Protocols, research document formulation and summary report interpretation, as well as medical support and data review for clinical trials during the research process. In addition, it also includes scientific support for other departments and external communication.

Clinical Research

• Develop appropriate programme profiles and programmes to support research recommendations and meet local registration requirements, and provide disease and programme training to CTA/CRC.
• Develop local ICF (informed consent document) and translate as required.
• Prepare and deliver product and program presentations at the investigator's meeting and answer questions from the investigator.
• Act as clinical director in the research team, review and approve subject eligibility and project deviation, review study medical data, analyze adverse events/serious adverse events and answer clinical and product inquiries from researchers.
• Provide input in the final determination of SAP (statistical analysis plan) and strive for database cleansing

Regulatory support

• Prepare clinical documentation as needed to respond to CDE query.
• Prepare slides as needed and deliver presentations to the CDE review meeting for the clinical section.

任职条件

Bachelor degree or above with major in clinical medicine/related

3 year's working experience in clinical medicine within at least 1 year's experience in clinical trial

2-3 year's experience in clinical protocol（Phase 1-3,prefer oncology project background

职位要求

• 学历要求：本科及以上
• 工作经验：5年以上
• 外语要求：英语读写/口语表达熟练

公司福利

• 福利年假 
• 带薪病假 
• 下午茶 
• 年度Outing 
• 年度体检 
• 团队建设 
• 交通及通讯补贴 
• 节日福利 
• 员工生日会