北京招聘

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 

任职资格： 

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 .

多年来一直专注于于为世界500强，跨国公司，国内上市公司提供管理咨询，人力资源咨询和中高端招聘服务，为中高级职业经理人提供更好的职业发展机会。
在中国服务力量遍布在北京、上海、广州、深圳、成都、南京、宁波、苏州等多个城市, 超过100名专业咨询顾问。