说明
该职位通过协调项目启动活动、创建全球程序、跟踪电子表格,以及生成并进行质量检查的 SAS 衍生数据集、表格、图形和数据清单,为临床开发项目提供支持。该职位还负责维护法规和 CDISC 相关知识,提供培训和指导,支持申报文件编制,并确保遵守 SOP、ICH-GCP 及适用法规。该职位要求熟练掌握 SAS,具备分析能力和沟通能力、注重细节,并能够在全球化且注重质量的环境中工作。
clinical research organizationsRaleigh, North Carolina
Parexel is a dedicated CRO providing the full range of Phase I to IV clinical development services. Its team of more than 24,000 global professionals works in partnership with biopharmaceutical leaders and sites to design and deliver clinical trials with patients in mind. Services include clinical, regulatory and therapeutic expertise, as well as market access planning and post-approval studies. Parexel says it has been a trusted global CRO and biopharmaceutical services company for over 35 years.