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Senior Scientist, Preclinical Research(FSP, 外派MNC)

3.5-4.5萬·13薪
  • 上海徐匯區(qū)
  • 虹梅路
  • 5-10年
  • 碩士
  • 全職
  • 招1人

雇員點(diǎn)評(píng)標(biāo)簽

  • 同事很nice
  • 工作環(huán)境好
  • 免費(fèi)班車
  • 人際關(guān)系好
  • 團(tuán)隊(duì)執(zhí)行強(qiáng)
  • 氛圍活躍
  • 交通便利
  • 管理人性化

職位描述

器械毒理
JOB SUMMARY
The individual will serve as a (key) scientific contributor for the development and execution of preclinical strategy. The
individual will contribute to/independently complete the design, execution, analysis and interpretation of preclinical studies to understand the safety and efficacy of products.
DUTIES & RESPONSIBILITIES
Under limited supervision and in accordance with all applicable China and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
Liaison with Business Partners
  • Provides preclinical scientific input on and assist to develop preclinical strategy as needed.
  • Communicates progress and milestone status to key stakeholders.
Preclinical Sponsor Oversight
  • Provides input and reviews for study protocols and reports from external preclinical studies.
  • Oversight of the study implemented in external labs to ensure compliance, scientific soundness, and integrity of the study.
Preclinical Study Execution
  • Planning and executing preclinical animal studies as needed.
  • Responsible for design of preclinical animal studies as needed.
  • Performs the role as designated Study Director as needed.
Responsible for ensuring compliance with all country, local and Company regulations, policies, and procedure.
Performs other duties assigned as needed?
Requirements:
Doctorate degree preferred in veterinary medicine, medical, biological sciences, biomedical engineering, and related major. Master’s degree required. At minimum 3 years of experience in preclinical research experience in a medical device or
pharmaceutical setting. GLP background is preferred.
Experience with large animal preclinical studies as study director is preferred.
General knowledge of Preclinical Research is required. Knowledge of NMPA regulations related to preclinical research is highly desired.
General knowledge of animal and human anatomy and physiology, surgical principles & theory, as well as biological
systems is highly desired.
Skills to develop tactics to successfully complete programs/projects/studies is required including trouble shooting skills.
Able to articulate scientific basis for decisions to project team partners.
Good communication skills to facilitate smoothly work cross functionally.
Good English communication (both written and verbal) skill is required.

工作地點(diǎn)

上海徐匯區(qū)新研大廈

職位發(fā)布者

孫靜/高招TA

昨日活躍
立即溝通
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康龍化成(北京)新藥技術(shù)股份有限公司(股票代碼:300759.SZ/ 3759.HK)是國(guó)際領(lǐng)先的生命科學(xué)研發(fā)服務(wù)企業(yè)。自2003年成立以來,康龍化成一直致力于人才培養(yǎng)和設(shè)施建設(shè),為包括小分子、大分子和細(xì)胞與基因治療藥物在內(nèi)的多療法藥物研發(fā)打造了一個(gè)貫穿藥物發(fā)現(xiàn)、臨床前及臨床開發(fā)全流程的研發(fā)生產(chǎn)服務(wù)體系??谍埢稍谥袊?guó)、美國(guó)、英國(guó)均開展運(yùn)營(yíng),擁有22,000多名員工,向北美、歐洲、日本和中國(guó)的合作伙伴提供研發(fā)解決方案并與之保持良好的合作關(guān)系。(詳情請(qǐng)?jiān)L問公司網(wǎng)站:www.pharmaron.com)
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