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CRAI-SCRA
8-27K/月上海市-上海/本科及以上/1-3年
陈祖萌一周前来过
江西亚麦嘉企业管理有限公司
职位详情
岗位职责
任职要求：
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
岗位职责：
外派阿斯利康
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
岗位职责：
外派阿斯利康
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
无
工作地点
- 上海市静安区西藏北路88号10楼
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公司信息
某医药公司
- 上海
- 1000-9999人
- 健康管理机构
- 民营
- 无
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2000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。 昆翎的历史可以追溯到1995年，公司在过去20多年里积累了深厚的临床研究专业经验和监管知识，并在中国、美国、欧洲、印度、日本和菲律宾等多个国家和地区开展了业务。昆翎在其发展旅程中经历过一系列的并购与重组，并成功的融入了昆翎医药、K&L咨询和iMedGlobal。未来，随着生命科学领域的创新发展，昆翎将继续为全球申办方在整个研发、注册和商业化阶段提供高质量的CRO服务。同时，公司将积极与成熟型和成长型的公司展开合作，依靠功能完善的CRO团队帮助申办方实现其本土和全球的战略目标。在全新品牌战略的引领下，昆翎将以“立足中国，服务全球”为己任，继续为全球制药、生物科技和医疗器械公司提供高质量、全方位服务的临床研究服务。 ●成就•迄今为止，昆翎已通过超过 70 家国际知名制药和医疗器械企业的稽查，参与并承担了超过 85 个创新药和近20 个生物类似物的注册申报、临床设计和开发工作•3 年内，昆翎已支持递交美国和欧洲新药证书申请 17 个，已获批 15 个•承接临床研究 1,600 余项，包括多个入组人数达 10,000 例以上的大型临床研究•全球布局的临床试验服务团队，承接国际多中心临床试验MRCT的能力完备•昆翎医药是中国目前创新药临床试验服务经验最为丰富的 CRO 公司之一•昆翎医药临床监查团队已与中国大陆、中国香港、中国台湾和韩国的多家医院建立了广泛联系，合作医院数量达到 1,500 余家•为中国大陆、中国香港、中国台湾和韩国等地的各阶段临床试验入组受试者近 300,000 例
