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藥物警戒專員-英語 Safety Associate Trainee

6000-8000元·13薪
  • 大連甘井子區
  • 1-3年
  • 本科
  • 全職
  • 招1人

職位描述

藥品警戒不良事件英語PV藥物警戒
崗位要求: 1. 本科及以上醫藥相關專業 2. 0-1年英語PV經驗 3. 良好的英語讀寫能力,口語好加分 Job Overview Manage the administrative support across all Lifecycle Safety service lines to the SO and LSM functions as appropriate. Provide support to junior administrative team members. Essential Functions ● Assist in processing of Lifecycle Safety data by collecting and tracking incoming Adverse Events(AE)/endpoint informatio, determining initial/update status of incoming events, tracking timelines for completion of event processing, distributing event information to appropriate project personnel in the workflow for continued processing, review and preparation of endpoint documentation, transfer of events to client and other parties as identified by operations lead, obtaining confirmation of report receipt and track submission and assuming workflow responsibilities for various projects. ● May assist with project workflow including database entry, quality control activities, and generation of Lifecycle Safety data reports, preparation of Lifecycle Safety submission dossiers, assisting with deadline quality measurements, as directed by operations team member or manager. ● Assist with administrative team support e.g. project start-up tasks, creation and maintenance of project files, systems access requests ● periodic distribution of AE listings ● and shipping of information supplies to sites as directed by senior operations team member. ● May coordinate, schedule and submit safety reports to regulatory authorities, marketing authorization holders, investigators, customers and operations team in accordance with deadlines ● perform project administrative tasks such as creation of labels using investigator list, maintenance of personal safety files for mail merges and regulatory documents, copying of documents, envelope stuffing, tracking and filing of submission dossiers, and distributing listings to client and/or operations team members. ● Creating, maintain and track case folders, filing, retrieving and distribution of case folders to operations team members, assisting in maintenance of document control storage and relevant applications/systems as directed. ● Archiving case folders and project files after event closure, coordination of transfer of archived material to company/customer archive storage facilities after study closure, assisting in creation of records management processes and procedures, providing key input to operations team on acquisition and/or upgrade of records management application/systems and serving as liaison between Lifecycle Safety department and records management department. ● May assist with system support tasks such as utilizing design specifications, study form, and protocol to create project specific entry specifications and annotated project forms for database under guidance from operations lead and/or manager ● creating project tracking spreadsheets and associated tracking entry specifications ● assisting in database validation through performance of user testing ● performing ad hoc database searches for operations team leads ● assisting operations team member in assessing database setup needs ● assist with project phone/fax line set-up as required ● escalating any system/equipment problem. ● Oversee and co-ordinate administrative support by coordinating team/department/customer/project oversight group meetings, coordinating stationery orders, dispatching documents via courier services, reserving meeting rooms and IT equipment ● and providing administrative support where required. Identify and record process or quality problems and bring them to the attention of a senior team member. ● Provide training/mentoring to new/less experienced staff. ● Participate in continuous improvement of all departmental processes and procedures by identifying and implementing efficiencies in workflow and/or case processing. ● Co-ordinate, oversee and delegate resource tasks to administrative team members as appropriate and monitor the intake of cases and archiving process when multiple coordinators are involved. ● Involvement and contribution in local/global department committees ● Perform other duties as assigned. Qualifications ● High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences ● 2 years’ relevant work experience. ● r equivalent combination of education, training and experience. ● Good understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Standard Operating Procedures (SOPs) and work instructions applicable to the role.. ● Good working knowledge of Microsoft Office and web-based applications. ● Good knowledge of medical terminology. ● Strong organizational skills and time management skills. ● Strong verbal/written communication skills. ● Self-motivated and flexible. Excellent attention to detail and accuracy. ● Ability to follow instructions/guidelines, utilize initiative and work independently. ● Proven ability to multi-task, manage competing priorities and deadlines. ● Willingness and aptitude to learn new skills across all Lifecycle Safety service lines.

工作地點

大連甘井子區騰飛軟件園1期

職位發布者

宋女士/HR

剛剛活躍
立即溝通
公司Logo艾昆緯醫藥科技(上海)有限公司
IQVIA(紐交所代碼:IQV)是全球專注生命科學領域的高階分析、技術解決方案和臨床研究服務供應商。IQVIA利用深入分析、前沿技術、大數據資源和廣泛領域的專業知識,智能連接醫療生態的各個環節。IQVIA Connected Intelligence?快速敏銳地為客戶提供強大的數據洞察,幫助客戶加速創新醫療的臨床開發和商業化進程,以更好的醫療成果惠及患者。IQVIA擁有約72,000名員工,足跡遍布100多個國家/地區。IQVIA擁有多元化的加強型隱私技術和保障手段,能夠在保護個人隱私的同時對信息進行管理和分析,幫助醫療利益相關方有效開展精準療法,獲得更佳的療效。這些洞見和能力能夠幫助生物科技、醫療器械、制藥公司、醫學研究者、政府機關、支付方以及其他醫療利益相關方,獲得對疾病、人類行為和科技進步更深入的理解,共同朝著治愈各類疾病的方向邁進。
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