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LTD-TOX-臨床前藥物安全評(píng)價(jià)專(zhuān)題負(fù)責(zé)人

1.3-2.5萬(wàn)
  • 蘇州吳中區(qū)
  • 3-5年
  • 碩士
  • 全職
  • 招1人

職位描述

崗位職責(zé):
1.Design and execute nonclinical toxicology study protocols, analyze and interpret the results, and write a final report of the findings;
2.Monitor all aspects of a study during the In Life phase;
3.Assure on-time delivery of high quality reports at the completion of each study;
4.Provide leadership and training to toxicology staff as required;
5.Provide input on equipment purchases intended for use in the toxicology program;
6.Remain current on appropriate company SOPs (standard operating procedures), GLP (Good Laboratory Practice) regulations, and regulatory guidelines.
任職要求:
1.MS in toxicology or related fields
2.Experience working directly with clients/patients and cooperatively in teams;
3.Experience designing/conducting/monitoring toxicology studies;
4.Demonstrated successful leadership and excellent written and oral communication skills;
5.Computer skills, particularly word processing, spreadsheet, and data acquisition software.

工作地點(diǎn)

蘇州市吳中區(qū)吳中大道1318號(hào)

職位發(fā)布者

呂女士/HR

今日活躍
立即溝通
公司Logo蘇州藥明康德新藥開(kāi)發(fā)有限公司
藥明康德（股票代碼：603259.SH/2359.HK）是國(guó)際領(lǐng)先的開(kāi)放式能力與技術(shù)平臺(tái)公司，為全球制藥及醫(yī)療器械等領(lǐng)域提供從藥物發(fā)現(xiàn)、開(kāi)發(fā)到市場(chǎng)化的全方位一體化的實(shí)驗(yàn)室研發(fā)和生產(chǎn)服務(wù)。本著以研究為首任，以客戶(hù)為中心的宗旨，藥明康德通過(guò)高性?xún)r(jià)比、高效率的服務(wù)平臺(tái)幫助全球客戶(hù)縮短藥物及醫(yī)療器械研發(fā)周期、降低研發(fā)成本。藥明康德平臺(tái)涵括化學(xué)藥研發(fā)和生產(chǎn)、細(xì)胞及基因療法研發(fā)生產(chǎn)、藥物研發(fā)和醫(yī)療器械測(cè)試等，正承載著來(lái)自全球30多個(gè)國(guó)家的3500多家創(chuàng)新合作伙伴的數(shù)千個(gè)研發(fā)創(chuàng)新項(xiàng)目，致力于將最新和最好的醫(yī)藥和健康產(chǎn)品帶給全球病患，實(shí)現(xiàn)“讓天下沒(méi)有難做的藥，難治的病”的夢(mèng)想。
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