
藥代動力學研究員-DMPK

職位描述
Responsibilities/Duties
? Support DMPK in vitro and/or in vivo assays including assay design, biosample analysis, method development and validation and report for various compounds and components in compliance with appropriate SOPs and regulatory agency guidelines.
? Support in setting up, validating, and conducting DMPK in vitro assays from protocol design, experiment, and report.
? Support in conducting and coordinating DMPK in vivo projects from protocol design, experiment, and report.
? Set up and performs method development and validation of various analytes in a variety of matrices with supervision.
? Set up, maintain, operate and perform routine and non-routine maintenance on general equipment, including problem identification and resolution.
? Inform Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect the integrity of the data and recommends corrective action.
? Suggest and perform modifications to test methods or procedures where precedence exists.
? Organize, conduct and evaluate analytical results and testing.
? Performs QC review of data.
? Maintain study documentation and laboratory records.
? Promote a cohesive team environment.
? Provide input and participate in project meetings, plans, monitors and guides project work.
? Maintain a clean and safe laboratory work environment.
? Train and assist less experienced staff.
? Participate in process improvement initiatives.
? Participate in client visits as needed, assist in communicating technical information.
? Effectively plan and utilize personnel and resources for timely completion of assigned projects.
? Assists in writing reports and protocols.
? Writes SOPs and methods.
? Assist in evaluation of data for incorporation into written reports.
? Perform other related duties as assigned.
Education/Qualifications
? BS/BA degree in science plus at least 3 years or above experience or MS degree with 1 years or above experience in analytical chemistry, pharmacokinetics, or metabolism.
Experience
? 1 years or above experience in analytical chemistry, pharmacokinetics, or metabolism
? Familiar with the use of standard laboratory equipment (e.g., balances, pipettes, centrifuges).
? Experience with use and trouble shooting of analytical equipment such as LC-MS/MS.
? Knowledgeable on a variety of study types, analysis procedures and methodologies.
企業(yè)簡介
科文斯,全球性的合同研究組織(CRO)Covance Inc.是全球服務最全面的藥物研發(fā)公司。
我們致力于推動醫(yī)療保健事業(yè)發(fā)展并實現(xiàn)Solutions Made Real?,通過向制藥公司和生物科技公司提供高質(zhì)量的非臨床、臨床前試驗、臨床和商業(yè)化服務,幫助減少藥物研發(fā)的時間和成本。憑借豐富的經(jīng)驗與深厚知識,我們具備獨特的優(yōu)勢,能為客戶合作伙伴提供不僅僅局限于測試的獨到見解。
我們還向化學品、農(nóng)用化學品和食品行業(yè)提供實驗室測試服務,同時也是毒理學分析服務、中心實驗室服務、藥物篩選服務的市場領(lǐng)導者,以及III期臨床試驗管理服務的全球頂級提供商。
科文斯官網(wǎng): https://www.covance.com/
職位發(fā)布企業(yè)

科文斯醫(yī)藥研發(fā)(北京)有限公司上海分公司
企業(yè)性質(zhì):外資企業(yè)
企業(yè)規(guī)模:5000-10000人
成立年份:2006
企業(yè)網(wǎng)址:www.covance.com
企業(yè)地址:上海市普陀區(qū)嵐皋路555號602-606室
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職位發(fā)布日期: 2018-12-12