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崗位職責(zé)
1. Lead/manage a team of biologists supporting in vitro screening of biologics; Establish robust and reproducible in vitro screening assays, technical platforms to evaluate biologics; review and validate novel drug targets for unmet medical needs in major disease areas, including oncology/immunology/metabolic diseases /CVD or a relevant major disease field.
帶領(lǐng)團(tuán)隊支持大分子藥物的體外篩選；負(fù)責(zé)創(chuàng)新藥物的分子及細(xì)胞水平體外篩選平臺建立，篩選項(xiàng)目方案設(shè)計、驗(yàn)證和優(yōu)化；負(fù)責(zé)對相關(guān)疾病靶點(diǎn)（腫瘤/免疫/代謝性疾病/心血管疾病等）進(jìn)行調(diào)研并做總結(jié)匯報。
2. As a project leader, lead drug discovery programs, responsible for setting up strategic direction and leading the program all the way to reach the milestone of approval of preclinical candidates. Coordinating various functions with different groups to drive the programs forward. Assisting in out-licensing/collaboration when needed.
作為項(xiàng)目負(fù)責(zé)人帶領(lǐng)大分子新藥研發(fā)項(xiàng)目，從靶點(diǎn)選擇到臨床前候選化合物（PCC）確定：負(fù)責(zé)方案設(shè)計，協(xié)調(diào)資源，和各部門合作推進(jìn)項(xiàng)目進(jìn)展直至PCC交付。
任職要求
學(xué)歷與專業(yè)
博士學(xué)歷，在腫瘤學(xué)/免疫學(xué)/代謝疾病/心血管疾病或相關(guān)領(lǐng)域擁有深厚知識。
工作經(jīng)驗(yàn)
5-10年大分子藥物研發(fā)經(jīng)驗(yàn)（工業(yè)界優(yōu)先）， 至少2年項(xiàng)目leader經(jīng)驗(yàn)。
具備批判性分析研究論文的強(qiáng)大能力，出色的領(lǐng)導(dǎo)能力和團(tuán)隊合作能力
需要在知名制藥/生物技術(shù)公司擁有相關(guān)藥物研發(fā)經(jīng)驗(yàn)