更新于 3月23日
职位描述
药品临床监查新药化学药生物药Ⅲ期Ⅱ期Ⅰ期
职责描述：
· Act as the main line of communication between the sponsor and the investigator
· Verifying that all research staff, facilities and investigational products have adequate qualifications and resources and these remain adequate throughout
· Responsible for the safety and proper conduct throughout the trial
· Verifying that the investigator follows the approved protocol and all GCP procedures
· Verifying that source data/documents and other trial records are accurate, complete, and maintained
· Adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol on the CRFs
· Experience should include monitoring skills. Prior relevant active independent field monitoring experience and site management experience
任职要求：
· Strong knowledge in ICH-GCP
· Ability to review and evaluate clinical data
· Computer literacy desirable
· Good oral and written communication skills
· Due to the nature of this position it may be required for the employee to travel
· Bachelor degree, or local equivalent, in medicine, science or related discipline
· Act as the main line of communication between the sponsor and the investigator
· Verifying that all research staff, facilities and investigational products have adequate qualifications and resources and these remain adequate throughout
· Responsible for the safety and proper conduct throughout the trial
· Verifying that the investigator follows the approved protocol and all GCP procedures
· Verifying that source data/documents and other trial records are accurate, complete, and maintained
· Adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol on the CRFs
· Experience should include monitoring skills. Prior relevant active independent field monitoring experience and site management experience
任职要求：
· Strong knowledge in ICH-GCP
· Ability to review and evaluate clinical data
· Computer literacy desirable
· Good oral and written communication skills
· Due to the nature of this position it may be required for the employee to travel
· Bachelor degree, or local equivalent, in medicine, science or related discipline
工作地点
济南槐荫区山东第一医科大学附属肿瘤医院1
公司信息
昆翎(北京)医药科技发展有限公司
D轮及以上 · 1000-9999人 · 医药研发/生产外包（CXO）
已审核
公司介绍
昆翎（ClinChoice）是一家致力于为生物医药和医疗器械客户提供高品质一站式服务的临床阶段CRO，服务包括临床运营、项目管理、生物统计、数据管理、注册事务、医学事务和药物警戒。昆翎已经在中国、美国、欧洲、印度、日本和菲律宾建立了主要的临床交付中心，目前在全球拥有1800多名员工，其临床运营团队覆盖了亚、欧、北美等七个国家和地区。高盛直投部董事总经理、昆翎董事会成员许小鸥先生认为，“随着创新疗法在全球的增长，CRO公司提供高效、可靠的研发服务能力变得尤其重要。昆翎独特的价值主张结合了其对于本地市场的了解、国际药物研发的经验以及高效的团队执行能力。我们坚信公司强劲的管理层团队以及其高效的执行能力，将为昆翎的发展开启新的篇章。
工商信息
企业名称 昆翎（北京）医药科技发展有限公司
企业类型 有限责任公司（自然人投资或控股的法人独资）
法人代表 刘东
经营状态 存续
成立时间 2008-07-23
注册资本 100万元
认证资质
营业执照信息
