崗位職責(zé):
1. Manage the programming of clinical trial projects and provide valuable reference suggestions when formulating project timelines or making other decisions.
2. According to the trial protocol and statistical analysis plan, formulate detailed programming plans and implement the programming as planned to complete the delivery.
3. In line with the project protocol deviation management plan, develop the protocol deviation programming specification documents and implement the protocol deviation programming.
4. Design and develop macro programs to support the data analysis and reporting of complex clinical trials.
5. Cooperate with the staff of other departments to complete such tasks as data review, data transmission, data sorting and ad hoc statistical analysis.
1.管理臨床試驗(yàn)項(xiàng)目的編程,在制定項(xiàng)目timeline或其他決策時(shí)提供有價(jià)值的參考意見(jiàn);
2.按照試驗(yàn)方案及統(tǒng)計(jì)分析計(jì)劃,制定詳細(xì)的編程計(jì)劃,并按計(jì)劃實(shí)施編程,完成交付;
3.按照項(xiàng)目方案偏離管理計(jì)劃,制定方案偏離編程說(shuō)明文件,實(shí)施方案偏離編程;
4.設(shè)計(jì)和開(kāi)發(fā)支持復(fù)雜臨床試驗(yàn)數(shù)據(jù)分析和報(bào)告的宏程序;
5.配合其他部門人員完成數(shù)據(jù)審查、數(shù)據(jù)傳輸、數(shù)據(jù)整理和臨時(shí)統(tǒng)計(jì)分析等工作。
任職要求:
MSc,Epidemiology and Health Statistics,Epidemiology, Statistics,Biostatistics.Have three years or more working experience in statistical programming; possess relevant experience in the pharmaceutical R & D industry and experience in using statistical analysis software (such as SAS, R, etc.); be familiar with the basic knowledge of biostatistics or medical statistics and understand the basic knowledge related to clinical trials in drug R & D.
碩士及以上學(xué)歷,流行病與衛(wèi)生統(tǒng)計(jì)學(xué)/流行病學(xué)/統(tǒng)計(jì)學(xué)/生物統(tǒng)計(jì)學(xué)或其他相關(guān)專業(yè);有3年及以上統(tǒng)計(jì)編程工作經(jīng)驗(yàn);有藥物研發(fā)行業(yè)相關(guān)經(jīng)驗(yàn)和統(tǒng)計(jì)分析軟件(如SAS、R等)使用經(jīng)驗(yàn);熟悉生物統(tǒng)計(jì)學(xué)或醫(yī)學(xué)統(tǒng)計(jì)學(xué)基礎(chǔ)知識(shí)、了解藥物研發(fā)臨床試驗(yàn)相關(guān)基礎(chǔ)知識(shí)。