职位详情
年底双薪
带薪年假
午餐补助
定期体检
弹性工作
年度旅游
节日礼物
五险一金
为了让HR同事及时与您联系以便获得更快的简历反馈,请您登录精鼎医药官方网站jobs. Parexel搜索R0000022510 投递您的简历
Basic Qualifications:
BA/BSc or higher degree in Statistics, Mathematics, Computer Science, or other related scientific subject with strong analytic skills and at least three (3) years of relevant career statistical programming or software development experience in a clinical development environment.
Familiarity with drug development life cycle and excellent skills with the manipulation, analysis and
reporting of clinical trials data.
Ability to effectively perform complex statistical programming and related tasks
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural Partners.
Ability to work effectively on multiple tasks or projects.
Experience developing, testing, and documenting Enterprise-level utilities, including SAS macros.
SAS experience with extensive macro development.
Experience in a UNIX/Linux environment including the automation of tasks using scripting
Experience in the software development life cycle.
Experience in at least one of the following additional languages.( Python, Perl)
Technical writing ability for software development team use and end-user reference and training
material
Excellent oral and written English communication skills
其他信息
语言要求:英语
行业要求:全部行业
公司介绍
As one of the world's global clinical research organizations (CRO), we provide the clinical development capabilities and integrated consulting expertise it takes to streamline development every step of the way — faster and more cost-effectively. Our over 18,000 employees have a deep conviction in what we do, and together with our customers, we are shaping the next generation of therapies, one patient at a time. What we do, we do.
工商信息
以下信息来自
注册地址
中国(上海)自由贸易试验区商城路506号新梅联合广场写字楼二期12层、14层
统一社会信用代码
91310115737470728W