(Sr.) Clinical Quality Manager
職位描述
Typical Accountabilities: * Lead the design and implementation on assigned local quality management activities, including performing accompanied site visits, in-house quality checks and provide local management team with quality metrics and dashboard in DevOps. * Provide advice to DevOps staff on AZ procedural framework including local clinical procedural documents, applicable Quality & Compliance manual documents, and on international guidelines such as ICH-GCP, industry standards and local regulations. Drive the continuous optimization of CQM helpdesk to support DevOps colleagues with quality and efficiency. * Drive the development, publication, training, implementation, maintenance and archiving of Local Procedural Documents, ensuring compliance with global Clinical Procedural Documents management requirements. * Act as DevOps contact with QA to design audit strategy to DevOps relevant activities and coordinate the audit conduct with study teams. Act as quality expert to advise DevOps staff on the resolution of the findings in audit and inspection reports. Lead trend analysis and lessons learned sharing on audit and inspection findings to relevant DevOps staff. * Lead local training platform and/or training programs from design to execution and drive continuous optimisation. * Lead DevOps clinical compliance management relevant activities, such as data privacy and cross boarder data transfer relevant assessment and contribute to process review to ensure business compliance with China local regulations.Education, Qualifications, Skills and Experience: * Bachelor’s degree in healthcare-related field, or equivalent. * At least 6 years experience in Clinical Operations or other related fields, including 2 years experience in clinical quality management or equivalent. * Solid knowledge and experience in China GCP inspections and deep understanding of GCP. * Good knowledge of Study Management, site management & monitoring, and local regulations. * Fluent spoken and written English. * Ability to look for and drive more efficient and effective methods/processes of delivering quality management activities. * Good communication and leadership to drive cross functional projects/initiatives. * Rapid learning and flexibility, high sense of responsibility and strong results orientation.
企業(yè)簡(jiǎn)介
阿斯利康是全球領(lǐng)先制藥公司,由前瑞典阿斯特拉公司和前英國(guó)捷利康公司于1999年合并而成。阿斯利康在6大治療領(lǐng)域?yàn)榛颊咛峁└挥趧?chuàng)新,卓有成效的醫(yī)藥產(chǎn)品,包括消化、心血管、腫瘤、中樞神經(jīng)、麻醉和呼吸等,其中許多產(chǎn)品居于世界領(lǐng)先地位。
阿斯利康總部位于英國(guó)倫敦,研發(fā)總部位于瑞典。產(chǎn)品銷售覆蓋全球100多個(gè)國(guó)家和地區(qū)。2005年公司銷售收入為240億美元。
阿斯利康擁有強(qiáng)大的研發(fā)能力,平均每個(gè)工作日的研發(fā)投入達(dá)到1400萬(wàn)美元 (2005年研發(fā)總投入為34億美元)。我們?cè)?個(gè)國(guó)家設(shè)有11個(gè)研發(fā)機(jī)構(gòu),共有11,900名員工從事與新藥研發(fā)相關(guān)的工作。
阿斯利康擁有極具希望的早期開(kāi)發(fā)產(chǎn)品組合,共有45個(gè)項(xiàng)目處于臨床前研究階段、17個(gè)項(xiàng)目處于一期臨床研究階段、13個(gè)項(xiàng)目處于二期臨床研究階段、6個(gè)項(xiàng)目處于三期臨床研究階段。
阿斯利康在全球19個(gè)國(guó)家有27個(gè)生產(chǎn)基地,共有14,000名員工致力于為客戶提供安全、有效、高質(zhì)量的產(chǎn)品。
阿斯利康在全球共有65,000名員工,從事醫(yī)藥產(chǎn)品和醫(yī)療服務(wù)的研發(fā)、生產(chǎn)和銷售業(yè)務(wù)。
阿斯利康被列入道瓊斯可持續(xù)發(fā)展指數(shù)(全球)以及顯示企業(yè)良好社會(huì)責(zé)任度的富時(shí)社會(huì)責(zé)任指數(shù)(FTSE4Good Index)。
職位發(fā)布企業(yè)

阿斯利康制藥公司
企業(yè)性質(zhì):
企業(yè)規(guī)模:1-49人
成立年份:
企業(yè)網(wǎng)址:http://m.chnequestrian.com
企業(yè)地址:海淀區(qū)
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職位發(fā)布日期: 2025-03-31