北京招聘QCD Scientist/Clinical Pharmacokineticist

QCD Scientist/Clinical Pharmacokineticist

精鼎医药研究开发（上海）有限公司

公司规模：10000人以上
公司性质：外资(欧美)
公司行业：制药/生物工程

职位信息

发布日期：2019-01-28
工作地点：上海-浦东新区
招聘人数：1人
工作经验：无工作经验
学历要求：招1人
语言要求：不限
职位月薪：50-60万/年
职位类别：生物工程/生物制药

职位描述

Come work with some of the best and most experienced in the Industry!With over 200+ years of combined cumulative experience, PAREXEL’s Quantitative Clinical Development (QCD) team is comprised of some of the best in the Industry, and their team’s experience is in high-demand! As a result of continued success, the team is expanding! We are currently seeking a QCD Scientist/Clinical Pharmacokineticist to join this highly recognized and distinguished team. In this tremendous opportunity the QCD Scientist will work alongside some of the preeminent experts in the Industry, work in diverse therapeutic areas and various disease states, work across all phases of clinical development, interact with the FDA and other Global Health Authorities; perform complex services for clients; and experience incredible professional growth.The QCD Scientist will ensure the strategic application of Clinical Pharmacokinetic (PK), Pharmacodynamic (PD), and Modeling & Simulation (MS) principles towards efficient drug development; will provide support for PK/PD strategy and interpretation to other SBUs and clients; and will provide quality services to clients.Additionally, the QCD Scientist will also: Analyze clinical PK/PD data as a member of several multidisciplinary development program teamsWork with clinical teams to design PK/PD components in various study designs such as first-in-human, bioequivalence and drug-drug interaction studiesContribute to clinical PK/PD sections of relevant documentsContribute to the design, analysis, reporting, and presentation of PK/PD modeling and simulation initiatives, including population PK/PD analyses for all phases of developmentReview scientific documentation including Clinical Study Protocols, SOPs, Statistical Analysis Plans and Clinical Study ReportsMaintain a working knowledge of pharmacology, biology, therapeutics, drug metabolism, bioanalysis, and biopharmaceuticsDevelop and maintain a relationship with internal and external clients and scientistsMaintain a positive, results orientated work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced and objective mannerReviewing/Authoring scientific publications, abstracts, postersParticipate in Business Development activities to represent QCD services

*Qualifications : To ensure success, the QCD Scientist will have: Strong knowledge of PK and PD principlesExperience with the design and implementation of Model-Based Drug Development strategiesKnowledge of Pharmacometric methodologiesExperience in Pharmacokinetic modeling Software such as Phoenix WinNonlinExperience in other software such as NONMEM, GastroPlus and R is desirable Excellent interpersonal, verbal and written communication skillsStrong clinical/scientific writing skillsClient focused approach to work Exhibit and promote a flexible attitude with respect to work assignments and new learning The ability to manage multiple and varied tasks with enthusiasmThe willingness to work in a matrix environment and to value and promote the importance of teamworkA minimum of 3-5 years’ experience in drug developmentStrong written and spoken English communication skillsStrong written and spoken Mandarin Chinese communication skills are highly preferredAn advanced science degree (MS, PharmD, PhD, MD) and/or relevant experienceThe ability to travel internationally for extended periods of time and/or the willingness to consider an secondment in China or other country within the APAC region

职能类别：生物工程/生物制药

公司介绍

精鼎医药（Parexel International）是全球领先的药物研究合同委托机构（CRO），总部位于美国生物医药圣地马萨诸塞州的波士顿附近，在世界各地拥有71个办事处，约17,600 名员工，为超过100个国家的客户提供服务。

精鼎医药成立于1982年，在三十多年的历程中，一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商，并且取得了卓越成果。目前，我们能够提供全世界CRO领域全面的新药临床阶段研发服务，服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。

将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案，可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。

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