崗位職責(zé):
1.在上級(jí)的指導(dǎo)下協(xié)助制定實(shí)驗(yàn)方案;
Assisting designing study plan under the guidance of superior;
2.負(fù)責(zé)參與新藥的藥代動(dòng)力學(xué)試驗(yàn)的具體實(shí)施、生物樣品分析,數(shù)據(jù)整理和報(bào)告撰寫(xiě);
Responsible for participating in conducting PK experiments, biological sample analysis, data sorting and report writing;
3.配合相關(guān)人員完成實(shí)驗(yàn)報(bào)告撰寫(xiě)及藥品注冊(cè)申報(bào)資料準(zhǔn)備;
Assisting writing study reports and the IND/NDA application documents;
4.負(fù)責(zé)參與臨床前制劑篩選和體系搭建;
Responsible for participating in preclinical formulation screening and platform development;
5.完成上級(jí)安排的其他任務(wù)。
Assisting your superior with other tasks.
任職要求:
1.碩士,藥代動(dòng)力學(xué)、生物樣品分析或相關(guān)專(zhuān)業(yè),1年以上工作經(jīng)驗(yàn);
MS in pharmacokinetics or related disciplines with 1+ year training/working experience;
2.熟練掌握LC/MS/MS等儀器、WinNonlin軟件的使用;
Good command of LC/MS/MS instruments and WinNonlin software;
3.具有良好的查閱及總結(jié)國(guó)外文獻(xiàn)的能力;
Good skills in searching and collecting information;
4.具有優(yōu)良的團(tuán)隊(duì)協(xié)作精神,工作積極主動(dòng)、創(chuàng)新精神。
Good collaboration, motivation and innovation;
5.熟練使用PPT、Word、Excel、Prism等工作軟件。
Good practice in the use of PPT, Word, Excel and Prism softwares.