職位描述
此職位為美斯達 http://www.macrostat.com.cn/ 發布 Responsibilities工作職責1.參與臨床開發計劃的準備Collaborates in the preparation of the clinical development plan.2.審閱病例報告表，確保其收集的信息可以滿足研究目的和標準Reviews case report forms to ensure that protocol objectives are met and project standards are maintained.3.制定或審閱統計分析計劃Statistical analysis plans development and review. Develops statistical programs as necessary to perform analysis and prepare data displays.4.必要時編寫統計分析程序，并呈現數據情況Develops statistical programs as necessary to displays data 5.參與數據核查報告的準備Participation the Data Review Report preparation6.撰寫統計分析報告 Preparation the statistical analysis report.7.參與審閱臨床研究報告的統計學部分Participant to review the statistical results in the clinical study report.8.為臨床研究結果的公開發表提過支持Provides support for publication of clinical trial results.9.通過查閱文獻、出現學術專題研討會和專業會議，追蹤統計學、藥物研發和管理指南的最新動態。Keeps abreast of new developments in statistics, drug development, and regulatory guidance through literature review and attendance at workshops and professional meetingMinimum Qualifications最低任職資格(a) Academic / Major 學歷 /專業BS，MS of statistics or biostatistics 統計或生物統計學士或碩士.(b) Professional Skills 專業技能要求Proficiency in SAS programming and statistical knowledge熟練掌握SAS編程及統計學相關知識。(c) Working Experience 工作經驗要求 BS with minimum 2 years，MS with 1 year, of pharmaceutical or CRO experience.本科學歷2年以上工作經驗，或碩士學歷，或者有CRO或者醫藥企業工作經驗。(d) Language ability 語言能力 Proficient in both Chinese and English. 中英文均佳。(e) Computer Literacy 電腦相關知識 SAS, MS Word and Excel.
