职位描述
职位要求：英语口语精通，生物统计专业背景，留学硕士或博士经历，至少1年生物统计工作经验，临床药学CRO经验优先。*Job Description
? Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques. ? Understand and apply moderately advanced statistical methods. ? Coordinate and lead a project team to successful completion of a project within given timelines and budget. ? Interact with clients as key contact with regard to statistical and contractual issues. ? Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents. ? Check own work in an ongoing way to ensure first-time quality. ? Provide training in statistical analysis to internal clients. ? Proactively participate in and/or lead process/quality improvement initiatives. ? Mentor and train junior members of the department. ? Support of Business Development, e.g. by attending and preparing bid defense meetings. ? Travel to, attend and actively contribute to all kind of client meetings as appropriate (e.g. discussing analysis concepts, presenting and discussing study results) ? Additional responsibilities as defined by supervisor/mana
*Job Qualifications
Good analytical skills ? Good Project Management skills ? Professional attitude ? Attention to Detail ? A good understanding of statistical issues in clinical trials ? Prior experience with SAS Programming required ? Ability to work independently ? Good mentoring / leadership skills
