职位信息
RESPONSIBILITIES ICSR Management - Records, processes, and conducts follow up and translates adverse events and other safety information from spontaneous and solicited sources. - Performs ICSR expedited reporting according to the local requirements. - Ensures local-language medical or scientific literature review. - Implements an appropriate local quality control (QC) procedure to ensure quality of information entered and reporting decisions. - Completes AE reconciliation and ensures AE identification effectiveness sampling consistent with global procedures. Periodic Safety Reporting - Prepare periodic safety reports (e.g., PSUR)., local annexes, local variations, and translation of safety deliverable documents. - Ensures submission of periodic safety reports and ensures documentation of evidence. Audits and Inspections Management - Actively assists in managing internal PV audits, audits of affiliate service providers/third parties and Regulatory Authority PV Inspections. - Actively assists in the development of CAPA in response to observations and the tracking actions to completion in a timely manner. Partnership with business partner with possibility for identification and/or handling of safety information - Ensures all PV requirements are in place for activities where there is a reasonable possibility for the identification and/or handling of safety information in accordance with AbbVie procedures and local requirements. PV Training - Ensures overall training compliance with corporate procedures and local PV requirements, including the maintenance of the PV Training Matrix and the development of additional PV training materials, as required. Legislation Intelligence - Monitors local (and applicable regional/area) PV-relevant hard intelligence, leading the impact assessment of them. Metrics and Oversight of the Pharmacovigilance System - Supports the provision of metrics that will ensure oversight of all aspects of the performance and functioning of the PV system in compliance with local regulations and internal company timelines/standards. Quality Management System - Develops and maintains local/regional procedures in line with corporate procedures and local requirements. - Performs the impact assessment of new/updated corporate policies, process, and procedures. - Actively assists with the PV Exception Reporting/CAPA process. - Actively assists with the business continuity plan and testing. - Develops and maintains the local PSMF in line with AbbVie’s PV system master file, when required by local/regional regulations INTERNAL / EXTERNAL CONTACTS AND INTERACTIONS - Affiliate medical, regulatory affairs, clinical, quality assurance and customer service personnel. - Affiliate Marketing, Sales and Operations personnel to ensure that all employees are trained and understand their responsibilities for reporting of any safety information. - National Regulatory Agency responsible for product safety. - Healthcare Practitioners, consumers, and patients. IDEAL CANDIDATE - Medical, pharmacy or life-sciences degree (or equivalent). - Effective communicator and able to work effectively in teams and a cross functional environment. - High customer orientation - Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity - Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency. CRITICAL SUCCESS FACTORS - Builds and maintains strong relationships with affiliate colleagues (e.g. Medical Affairs, Regulatory Affairs, Commercial) and PPS and tailors communication to different stakeholders to enhance understanding of PV requirements and elevate the PV internal brand. - Learns fast, grasps the “essence”, ability to manage complexity and changes to change course quickly where indicated to add value to the PV system. - Acts consistently with AbbVie’ s ethics, obligations and local laws – putting patient safety, partnerships and overall AbbVie’s interests before individual, immediate team and functional interests. - Focused on compliance; identifies, manages and escalates issues in a timely manner.
公司信息
关于艾伯维中国
艾伯维(纽约证交所:ABBV)是一家于2013年1月2日正式成立的全球研究型生物制药公司,从雅培公司拆分而来。 艾伯维将尖端生物科技与百年传承的专注、激情,以及专业技术和组织架构集于一身,凭借其专业技术、敬业的员工和独特的创新方式,旨在研发并推广先进治疗方法,解决世界范围内的一些疑难杂症。2013年,全新成立的艾伯维在全球范围内拥有近21,000名员工,产品销往170多个国家。
艾伯维已在中国正式注册成为一家外商独资的医药公司,并且于2013年6月1日完成与雅培中国的拆分。艾伯维中国的产品线涉及多个疾病领域,涵盖免疫学领域、抗病毒学领域、***学领域以及麻醉学领域。同时,艾伯维与中国的医学界和政府部门紧密合作,共同开展覆盖丙肝、肿瘤、免疫学、神经科学、疼痛和妇科健康等领域的临床研究。
艾伯维中国介绍
中国总部 上海
研发中心 艾伯维中国研发中心——上海张江研发中心,落成于2009年3月,是艾伯维全球7个研发中心之一。作为临床前研究的一环,支持全球药品研发中心(GPRD)的药物研发,主要集中在免疫、疼痛、神经系统与肾病领域。
员工数 近500名
历史 艾伯维中国成立于2013年6月1日
企业评级
艾伯维被纳入标准普尔500红利经典指数(S&P 500 Dividend Aristocrat Index) ,纳入这一指数的标准是公司股票连续25年以上实现持续增长的现金分红。同时, 艾伯维也被纳入标准普尔高产红利经典指数(S&P High Yield Dividend Aristocrats Index) ,纳入这一指数的标准是连续20年以上实现持续增长的现金分红。
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