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Associate Manager, Clinical Operations
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職位描述
職位描述:
1.Actsas the China/Regional Lead for the designated global/regional studies andassists the Senior Manager/Manager, Clinical Operations in the dailyoperational matters related to the execution, management and monitoring of thetrials, such as review of informed consent forms, participating in site PSSVs,co-monitoring visits, close-out visits, drafting of these visit reports, reviewof IMP packages, etc. so as to ensure that the defined timelines and milestonesare being met in a timely and efficient manner.
2.Assiststhe global/regional project teams to provide technical and content expertisewithin China/Asia Pacific region during the course of the study, as well as identifyingpotential challenges and working with team to strategize possible solutions.
3.Assists the Senior Manager/Managerof Clinical Operations in CDD to enhance process, functional and operationalefficiencies in the clinical development of their designated global/regionaltrials through sharing of information, best case examples etc. within CDD andacross the different PCUs
4.Provides general CRO/vendoroversight in the management and progress of their designated global/regionaltrials in China/Asia Pacific region
5.Participates in projectsand initiatives relating to better understanding of patient reality and hhcwithin area of work
6.Assist in the improvementof EPCS committees and processes, wherever possible.
Qualificationsand Expertise
· Working knowledge of entire drug developmentprocess, including clinical plan development and execution of entire clinicalstudy chain, specifically within the China/Asia Pacific region
· Detailed knowledge of Code of Federalregulations (CFRs), ICH guidelines, clinical operations, project management,and corporate /regional SOPs
· Demonstrated ability to manage and coachreports who are CRO project managers and individual contributors
· Good organizational, time management andattention to detail skills
· Extremely proficient computer skillsincluding MS Word, Excel, and PowerPoint
Strong verbal,written and interpersonal communication skills, especially needed to workeffectively in a cross-functional and cross-cultural team environment, managingthat team as required企業(yè)簡介
日本衛(wèi)材株式會社是一家以研究開發(fā)醫(yī)藥產(chǎn)品為主的跨國公司,總部設(shè)在日本東京,始建于1941年,其海外分支機(jī)構(gòu)、子公司和工廠分布于歐洲、美洲和亞洲各地。作為一家立足于科研的醫(yī)藥公司,我們十分重視產(chǎn)品研發(fā)工作。以筑波研究所為協(xié)調(diào)中心,大約有1300名研究者在全球晝夜不停的工作,開發(fā)下一代有創(chuàng)造性的新藥,滿足亟待解決的醫(yī)學(xué)需求。我們致力于神經(jīng)病學(xué)、胃腸病學(xué)以及腫瘤學(xué)專業(yè)領(lǐng)域的研究。為了涉足未來的專業(yè)領(lǐng)域,我們還在不斷把研究拓展到新興的前沿學(xué)科。
衛(wèi)材(中國)藥業(yè)有限公司是由日本衛(wèi)材株式會社全額投資成立的獨(dú)資制藥企業(yè)。衛(wèi)材(中國)的生產(chǎn)工廠位于蘇州工業(yè)園區(qū)內(nèi),總投資額1.1億美金,占地25,000平方米。
衛(wèi)材(中國)秉承hhc的企業(yè)宗旨,以Compliance(遵守道德)為行為準(zhǔn)則,以GMP為質(zhì)量標(biāo)準(zhǔn),向患者及其家屬提供高質(zhì)、環(huán)保、安全、滿意的產(chǎn)品以及服務(wù)的同時,積極回報社會,為促進(jìn)中國醫(yī)藥市場的健康發(fā)展不懈努力著。目前,衛(wèi)材在中國的產(chǎn)品主要有“彌可保”、“敏使朗”、“安理申”、“波利特”、“施維舒”、“能氣朗”、“妙納”等。
配合在華業(yè)務(wù)的快速發(fā)展,成長中的衛(wèi)材中國誠邀更多有志之士加入!
我們提供的不僅僅是一份職業(yè),而是您事業(yè)發(fā)展的機(jī)會!
職位發(fā)布企業(yè)
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衛(wèi)材(中國)藥業(yè)有限公司
企業(yè)性質(zhì):民營企業(yè)
企業(yè)規(guī)模:100-499人
成立年份:1941
企業(yè)網(wǎng)址:www.eisai.com.cn/
企業(yè)地址:南京西路1601號越洋廣場39-40F
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職位發(fā)布日期: 2016-12-14