职位描述
此职位为美斯达 http://www.macrostat.com.cn/ 发布 Responsibilities工作职责1.参与临床开发计划的准备Collaborates in the preparation of the clinical development plan.2.审阅病例报告表，确保其收集的信息可以满足研究目的和标准Reviews case report forms to ensure that protocol objectives are met and project standards are maintained.3.制定或审阅统计分析计划Statistical analysis plans development and review. Develops statistical programs as necessary to perform analysis and prepare data displays.4.必要时编写统计分析程序，并呈现数据情况Develops statistical programs as necessary to displays data 5.参与数据核查报告的准备Participation the Data Review Report preparation6.撰写统计分析报告 Preparation the statistical analysis report.7.参与审阅临床研究报告的统计学部分Participant to review the statistical results in the clinical study report.8.为临床研究结果的公开发表提过支持Provides support for publication of clinical trial results.9.通过查阅文献、出现学术专题研讨会和专业会议，追踪统计学、药物研发和管理指南的最新动态。Keeps abreast of new developments in statistics, drug development, and regulatory guidance through literature review and attendance at workshops and professional meetingMinimum Qualifications最低任职资格(a) Academic / Major 学历 /专业BS，MS of statistics or biostatistics 统计或生物统计学士或硕士.(b) Professional Skills 专业技能要求Proficiency in SAS programming and statistical knowledge熟练掌握SAS编程及统计学相关知识。(c) Working Experience 工作经验要求 BS with minimum 2 years，MS with 1 year, of pharmaceutical or CRO experience.本科学历2年以上工作经验，或硕士学历，或者有CRO或者医药企业工作经验。(d) Language ability 语言能力 Proficient in both Chinese and English. 中英文均佳。(e) Computer Literacy 电脑相关知识 SAS, MS Word and Excel.
