武汉招聘

Clinical Programmer (SAS programmer)

Clinical Programmer develops SAS programs to create datasets and tables, listings, and graphics according to the statistical analysis plan. This role requires an understanding of the clinical trial analysis and reporting, and the ability to apply knowledge of the SAS® statistical programming application along with knowledge of industry-accepted standards, including CDISC SDTM and ADaM.

Responsibilities include but are not limited to:

Develop SAS programs to create SDTM/ADaM datasets, and create statistical tables, listings, and graphics (TLGs) according to the statistical analysis plan

Assist Statistician & Lead Programmer to develop specifications, Statistical Analysis Plan (SAP), and TLG mock up.

Perform quality control and/or validation of other programmers’ outputs

Participate in statistical analysis plan, data validation plan, data management plan and blind data review

Qualifications

graduate degree, preferably in life science and/or healthcare professional

Must read, write and speak fluent English, good written and oral communication skills

Strong team player; service-oriented mindset

WuXi PRA Clinical Research (Shanghai) Co., Ltd. offers comprehensive Phase I-IV clinical trial services in Mainland China, Hong Kong and the Asia region. With 5 offices and staff based in 17 cities across China, WuXiPRA’s locally based project teams operate with the support of PRA’s global resources, clinical research expertise, global technologies and SOPs. This centralized operational approach promotes higher quality and outstanding client service. WuXiPRA has invested significantly in staff focused on CFDA regulatory expertise, project management and clinical informatics resources, as well as other support services, including RPS embedded strategic outsourcing.

上海康德保瑞医学临床研究有限公司在中国内地、香港及亚洲地区提供全方位的I-IV期临床试验服务。 康德保瑞在中国有5个办公室，员工分布在17个城市，其团队拥有保瑞医药丰富的全球资源和临床研究专业知识以及全球化的技术和标准操作规程支持。这些有助于全球性、区域性以及本土的临床试验运作达到更高的质量。康德保瑞在人员方面投入巨大，主要集中在CFDA注册专业知识、项目管理、临床信息资源以及包括战略外包服务的其它支持服务方面。