5 results for Statistical Programmer Jobs in Shanghai, Shanghai, CN

该职位来源于猎聘 至少1年SAS经验。 主要工作内容： Deliver best value and high quality service. Ensure quality control (QC) on all process and technical activities related to: - trial set-up and maintenance, and/or derived dataset, table, listing, and figure programming and/or implementation of system applications and upg...

Summary负责几项研究，中型到大型项目或项目级活动的所有统计编程/数据审查报告和分析开发方面。作为关键合作者和战略合作伙伴，确保药物开发计划得到有效执行，并及时和高质量的可交付成果。符合内部和监管指南的项目/研究标准和规范。监督编程风格，统计报告的质量以及时间表的遵守情况。About The RoleKey Responsibilities： Lead statistical programming activities as Trial Programmer for either a large/pivotal study or several studies, or act as a ...

该职位来源于猎聘 At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us ap...

该职位来源于猎聘 The key responsibilities of this role include but not limited to: ? Providing technical and project management leadership in analytical programming and application (SAS) designed to analyze and report complex clinical trial data and for electronic regulatory submissions and filings ? Collab...

该职位来源于猎聘 主要职责： 该职位将在统计编程和报告领域发挥领导作用。担任这一职务的人员将享受极具竞争力的薪酬和福利。积极进取、团队导向且质量至上的员工有可能晋升至技术或业务领导岗位。 及时、准确、高效地完成任务，确保质量和工作效率。交付成果需符合CDISC、FDA、EMA、CFDA、PMDA及其他监管机构的监管提交标准。工作包括但不限于以下内容： 1.领导研究团队，参与资源规划并管理时间表和交付成果。包括管理项目组成员的编程任务，并跟进任务状态，以确保按时高质量地完成交付成果。 2.准备SDTM数据映射规范、ADaM数据集规范、数据审查员指南和define.xml文件。对其他员工提供的此类...