长沙招聘

学历要求
统计学，计算机或数学相关领域大学本科及以上
硕士学位优先考虑

工作经验
具备三年临床研发领域的SAS编程经验
有临床开发与药品业务方面经验，了解临床和新药开发的相关程序。
具备协助新药申报的工作经验
拥有广泛的电脑系统﹑操作系统和用于支持临床项目的分析报告环境以及通过SDLC进行软件开发等方面的知识。

技能要求
熟悉医药科技现状和全球数据分析及报告系统，以有效的进行数据编程。
精通SAS编程语言
具备对内/对外及同事间有效的口头和书面沟通技巧
能够运用视窗操作系统，Word，Excel，Outlook
能够编写清晰标准，文档完整的计算机程序
具备按已定义的编程标准进行工作的能力
具备很强的分析能力
具备同时进行多个项目工作的能力
具备良好的基础能力，拥有面对学术和非学术听众的演讲经验
良好的书写能力进行有效的演示
能够熟练运用英语进行书面和口头的有效沟通
必备高度精确性，非常关注细节，及质量控制的工作方式
能够在多文化氛围下高效工作
能够在矩阵组织中工作
利用并分享创新的方案来建立和保持竞争优势
主动寻找合作机会并采取相应行动
以尊重的态度来挑战日常实践操作和决定以保证完整性和符合规范
愿意为一个学习型组织工作，鼓励进行尝试，承担风险，并在工作绩效的各方面寻求进步

Education
At least bachelor degree or equivalent in statistics, computer science, or a mathematical science
Master's Degree preferred
Experience
3 years relevant experience with SAS programming in clinical development
Some clinical development and business experience in order to have an understanding of the processes associated with clinical and regulatory operations.
Experience supporting regulatory submissions
Extensive knowledge of computer systems, operating systems and analysis and reporting environments used in the support of clinical programs and the development of software via structured SDLC.
Key Competencies
Strong understanding of the current technologies and global Analysis and Reporting environments to utilize them for efficient delivery of programming outputs.
Expertise in the SAS programming language.
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.

Basic knowledge to use Windows OS, MS-Word, MS-Excel, E-Mail (MS-Outlook).
Ability to write clear, well documented, and standardized computer programs.
A readiness and ability to work to pre-defined programming standards.
Strong analytical skills.
Able to work on multiple projects simultaneously.
Demonstrated platform skills. Experience in presenting to science and non-science audiences.
Demonstrated effective written communication skills
Capability to communicate effectively in English, both verbally and written.
Must be accurate and have an excellent attention to detail and a quality control approach to work.
Ability to work effectively in a multi-cultural context
Ability to work effectively in a matrix organization
Utilizes and shares innovative approaches to build and maintain a competitive advantage
Looks for opportunities for collaboration and acts upon them
Respectfully challenges practices, decisions or ideas to uphold integrity and ethical standards.
Contributes to a learning organization, encouraging experimentation, risk-taking, and development in all aspects of work performance.

简历接收邮箱：chinacpwtalent@pfizer.com

On October 31, 2005, Pfizer announced the official opening of China Research and Development Center (CRDC) in Shanghai. Pfizer Global Research and Development’s Center is mainly engaged in drug development activities. Much of the facility's capacity is devoted to the study design, data management and statistical analysis of global phase I-IV clinical trials, as well as the clinical study report process. In addition, CRDC is a part of Pfizer global Safety and Risk Management and covers the functions of safety data processing and assessment. The center also trains Pfizer employees in China and throughout the Asia region in internationally recognized Good Clinical Practice standards.
辉瑞公司于2005年10月31日宣布辉瑞中国研发中心正式在上海揭幕。辉瑞中国研发中心主要为全球辉瑞药物开发提供支持工作。大部分的功能是围绕在I-IV期临床试验研究设计、数据管理和生物统计分析、以及临床试验报告的部分准备工作。此外，该中心是辉瑞全球安全和风险管理部的一个分支，负责安全数据处理和评估工作。研发中心还将为辉瑞公司在中国及亚洲的其它运营部门的员工提供国际标准的临床试验管理规范(GCP)的技术培训。