1.負(fù)責(zé)制定臨床研究統(tǒng)計(jì)計(jì)劃，完成臨床試驗(yàn)方案中的統(tǒng)計(jì)部份設(shè)計(jì)，包括樣本量計(jì)算、隨機(jī)和編盲、統(tǒng)計(jì)分析計(jì)劃等；
2.參與方案討論會(huì)，并提供統(tǒng)計(jì)支持；
3.臨床數(shù)據(jù)統(tǒng)計(jì)分析與報(bào)告審核；
4.臨床研究統(tǒng)計(jì)部分供應(yīng)商管理，審核或獨(dú)立撰寫統(tǒng)計(jì)分析計(jì)劃，可獨(dú)立進(jìn)行研究數(shù)據(jù)的資料處理和統(tǒng)計(jì)分析；
5.能在工作中使用SAS等軟件進(jìn)行統(tǒng)計(jì)分析程序編寫，進(jìn)行一定的數(shù)據(jù)挖掘和分析；
6.能參與學(xué)術(shù)交流及藥物審評(píng)討論。

Key Responsibilities:
1.Develop and execute statistical plans for clinical trials, including sample size calculation, randomization, and blinding.
2.Provide statistical support during protocol discussions and meetings.
3.Conduct data analysis and review statistical reports.
4.Manage and oversee vendors handling statistical portions of clinical trials.
5.Utilize statistical software (e.g. SAS) for data mining, analysis, and reporting.

1.教育背景：博士學(xué)歷，生物統(tǒng)計(jì)、醫(yī)學(xué)統(tǒng)計(jì)、臨床等相關(guān)專業(yè)；
2.工作經(jīng)驗(yàn)：獨(dú)立完成過臨床數(shù)據(jù)收集、整理、挖掘分析工作；熟悉臨床試驗(yàn)設(shè)計(jì)與統(tǒng)計(jì)分析流程，2年以上相關(guān)經(jīng)驗(yàn)；優(yōu)秀應(yīng)屆生也可考慮；
3.專業(yè)技能：熟悉國內(nèi)外臨床試驗(yàn)相關(guān)的生物統(tǒng)計(jì)學(xué)技術(shù)指導(dǎo)原則，熟練運(yùn)用臨床試驗(yàn)常規(guī)統(tǒng)計(jì)軟件；
4.其他條件：有較強(qiáng)的邏輯性、強(qiáng)烈的團(tuán)隊(duì)合作意識(shí)與責(zé)任感，有較強(qiáng)的英文閱讀原文和寫作的能力。

Requirements:
1.Education: PhD in Bio-statistics, Medical Statistics , Clinical or related fields.
2.Experience: 2+ years of experience in clinical trial design and statistical analysis.
3.Skills: Proficient in using statistical software and familiar with domestic and international biostatistical technical guidelines related to clinical trials. With strong logic and responsibility in work.
4.Language: Fluent in English Reading and Writing.