職位描述
此職位為美斯達(dá) http://www.macrostat.com.cn/ 發(fā)布 Responsibilities工作職責(zé)1.參與臨床開(kāi)發(fā)計(jì)劃的準(zhǔn)備Collaborates in the preparation of the clinical development plan.2.審閱病例報(bào)告表，確保其收集的信息可以滿足研究目的和標(biāo)準(zhǔn)Reviews case report forms to ensure that protocol objectives are met and project standards are maintained.3.制定或?qū)忛喗y(tǒng)計(jì)分析計(jì)劃Statistical analysis plans development and review. Develops statistical programs as necessary to perform analysis and prepare data displays.4.必要時(shí)編寫(xiě)統(tǒng)計(jì)分析程序，并呈現(xiàn)數(shù)據(jù)情況Develops statistical programs as necessary to displays data 5.參與數(shù)據(jù)核查報(bào)告的準(zhǔn)備Participation the Data Review Report preparation6.撰寫(xiě)統(tǒng)計(jì)分析報(bào)告 Preparation the statistical analysis report.7.參與審閱臨床研究報(bào)告的統(tǒng)計(jì)學(xué)部分Participant to review the statistical results in the clinical study report.8.為臨床研究結(jié)果的公開(kāi)發(fā)表提過(guò)支持Provides support for publication of clinical trial results.9.通過(guò)查閱文獻(xiàn)、出現(xiàn)學(xué)術(shù)專(zhuān)題研討會(huì)和專(zhuān)業(yè)會(huì)議，追蹤統(tǒng)計(jì)學(xué)、藥物研發(fā)和管理指南的最新動(dòng)態(tài)。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(xué)歷 /專(zhuān)業(yè)BS，MS of statistics or biostatistics 統(tǒng)計(jì)或生物統(tǒng)計(jì)學(xué)士或碩士.(b) Professional Skills 專(zhuān)業(yè)技能要求Proficiency in SAS programming and statistical knowledge熟練掌握SAS編程及統(tǒng)計(jì)學(xué)相關(guān)知識(shí)。(c) Working Experience 工作經(jīng)驗(yàn)要求 BS with minimum 2 years，MS with 1 year, of pharmaceutical or CRO experience.本科學(xué)歷2年以上工作經(jīng)驗(yàn)，或碩士學(xué)歷，或者有CRO或者醫(yī)藥企業(yè)工作經(jīng)驗(yàn)。(d) Language ability 語(yǔ)言能力 Proficient in both Chinese and English. 中英文均佳。(e) Computer Literacy 電腦相關(guān)知識(shí) SAS, MS Word and Excel.
