崗位職責(zé):
崗位職責(zé):
1.負(fù)責(zé)藥物發(fā)現(xiàn)及開(kāi)發(fā)階段的藥代動(dòng)力學(xué)項(xiàng)目管理工作,與客戶(hù)交流體內(nèi)、體外等實(shí)驗(yàn)需求(包括實(shí)驗(yàn)設(shè)計(jì)、存在問(wèn)題以及可能風(fēng)險(xiǎn)),達(dá)成一致意見(jiàn)并提供實(shí)驗(yàn)方案;
2.高效執(zhí)行項(xiàng)目管理:與實(shí)驗(yàn)組、報(bào)價(jià)組、銷(xiāo)售以及其他功能組或部門(mén)密切交流,確保項(xiàng)目按預(yù)定方案和計(jì)劃開(kāi)展。與客戶(hù)及時(shí)溝通項(xiàng)目進(jìn)度,組織、協(xié)調(diào)、幫助解決項(xiàng)目問(wèn)題;
3.審閱實(shí)驗(yàn)結(jié)果和報(bào)告并給客戶(hù)提供合理的數(shù)據(jù)解讀,組織回復(fù)客戶(hù)疑問(wèn);
4.幫助組織客戶(hù)來(lái)訪、核查等準(zhǔn)備工作。
Accountabilities:
1.Be responsible for the project management of drug discovery and development stage, communicate in vivo and in vitro experimental requirements (including experimental design, existing problems and possible risks) with clients, reach consensus and provide experimental protocol;
2.Efficient Project Management: Interacts closely with experimental groups, quoting groups, sales, and other functional groups or departments to ensure that the project is conducted according to predetermined protocols and plans. Communicate project progress with clients in a timely manner, organize, coordinate and help solve project problems;
3.Review the test results and report and provide reasonable data interpretation for the client, and organize to reply to the client
s questions;
4.Help organize client visit, audit and other preparation work.
任職要求:
崗位要求:
1.藥代動(dòng)力學(xué)、藥理學(xué)、生物學(xué)、生物分析等相關(guān)專(zhuān)業(yè)碩士及以上學(xué)歷;
2.了解藥物研究與開(kāi)發(fā)流程,熟悉藥代動(dòng)力學(xué)相關(guān)實(shí)驗(yàn)平臺(tái)。
3.具有良好的學(xué)習(xí)能力,有較好的科研素養(yǎng)和解決問(wèn)題的能力;
4.具有良好的溝通、項(xiàng)目管理、時(shí)間管理能力,一定的抗壓能力;
5.具有良好的英文書(shū)寫(xiě)、聽(tīng)力和口語(yǔ)表達(dá)能力,有海外經(jīng)驗(yàn)者優(yōu)先。
您將得到的培訓(xùn):
1.平臺(tái):參與到從臨床前早期篩選到臨床早期開(kāi)發(fā)的藥物研發(fā)全過(guò)程;
2.跨部門(mén)交叉學(xué)習(xí):通過(guò)與藥化、生物、毒理、制劑、分析等部門(mén)的科學(xué)家們的緊密合作快速提升跨界知識(shí)技能;
3.全方位的培訓(xùn):系統(tǒng)化專(zhuān)業(yè)知識(shí)培訓(xùn)、多項(xiàng)目經(jīng)驗(yàn)學(xué)習(xí)分享、資深管理層教練式培養(yǎng)。
職業(yè)發(fā)展:
1.通過(guò)一體化研發(fā)項(xiàng)目熟悉藥物研發(fā)的全流程,可發(fā)展多學(xué)科交叉科研方向。
2.通過(guò)多管線、多階段項(xiàng)目管理的經(jīng)驗(yàn)積累,成為高級(jí)項(xiàng)目管理人才。
Requirement:
1.Master degree or above in DMPK, Pharmacology, Biology, Bioanalysis, etc.;
2.Understand the process of drug research and development, and be familiar with the experimental platform related to DMPK.
3.Have good learning ability, good scientific research literacy and problem-solving ability;
4.Have good communication, project management, time management ability, along with a certain level of resilience to stress;
5.Good English writing, listening and oral expression skills, with overseas experience is preferred.
Training you will receive:
1.Unique platform: participate in the whole process of drug R & D from preclinical early screening to clinical early development;
2.Cross-departmental learning: rapidly enhance interdisciplinary knowledge and skills through close collaboration with scientists from departments such as Medicinal Chemistry, Biology, Toxicology, Formulation, and Analytical Chemistry;
3.Comprehensive training: systematic professional knowledge training, multi-project experience learning and sharing, senior management coaching training.
Career Development:
1.Become familiar with the entire drug development process through integrated research projects, enabling the development of interdisciplinary research directions.
2.Accumulate experience in managing multi-pipeline and multi-stage projects to become a senior project management professional.