www.bhdu.cn-夜肉伦伦影院无码 ,国产精品www夜色视频,3d动漫精品啪啪一区二区免费,久久婷婷综合缴情亚洲狠狠

<blockquote id="4uc0g"><tfoot id="4uc0g"></tfoot></blockquote>
  • <fieldset id="4uc0g"><table id="4uc0g"></table></fieldset>
  • <fieldset id="4uc0g"><menu id="4uc0g"></menu></fieldset>
  • <ul id="4uc0g"><sup id="4uc0g"></sup></ul>
    <strike id="4uc0g"></strike>
    <del id="4uc0g"></del>
    <strike id="4uc0g"></strike>
    更新于 7月5日

    臨床項目啟動專員

    1.5萬-1.8萬·13薪
    • 北京大興區(qū)
    • 1-3年
    • 本科
    • 全職
    • 招1人

    職位描述

    SSU
    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
    Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
    That’s our vision. We’re driven by it. And we need talented people who share it.
    If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
    The Role:
    As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.
    ? Coordinate, balance and facilitate activities related to the completion of Critical Document Package (CDP) and the IP release checklist (SST004-SOP-F01) in accordance with ICH GCP guidelines and all applicable regulations, laws, ethical standards, other guidelines, sponsor requirements
    ? Ensure that the overall process is focused on quality, efficiency and cost containment for a particular region / sub division within the CDP group, under the general mentorship of Mgr/Sr. Manager – Central Services or Designee.
    What you need
    ? A high school diploma or local equivalent
    ? Bachelor’s Degree preferably in Life Sciences
    ? Minimum of 1 years’ experience or understanding of clinical study start up requirements and activities.
    ? Experience of Clinical Trial operations and meeting regulatory guidelines
    ? Proficient project management skills.
    Benefits of Working in ICON:
    Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
    We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
    We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
    But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
    ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
    If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

    工作地點

    宏達工業(yè)園

    職位發(fā)布者

    鐘奕姣/HR

    三日內(nèi)活躍
    立即溝通
    公司Logo愛恩康臨床醫(yī)學研究(北京)有限公司
    At ICON we believe that our people are the most important asset. It is they who have helped to make ICON the success it is. Their commitment to clients, quality and delivery has earned ICON its enviable reputation. About DOCS: DOCS- ICON Resourcing Solutions is a division of ICON plc that provides global staffing solutions to Pharmaceutical, Biotechnology, Medical Device companies and CROs in over 39 countries. We can recruit in virtually any location having access to offices in over 25 countries. This truly makes DOCS a company with global reach and personal focus. ICON has been in APAC since 1996 and the DOCS division of ICON is now expanding in the APAC region. Our Services: We are a specialist recruitment division focusing in Clinical Research, Medical Affairs, Regulatory Affairs, Drug Safety, Health Economics, Data Management& Statistics, Quality Assurance etc. Our full-spectrum resourcing solutions extend from contingent staffing, to functional resourcing, large-scale FSP and executive search. In addition, DOCS has developed a tailored training division‘CRAcademy’ to provide Traineeships and Training. We can recruit in virtually any location having access to offices in over 25 countries. This truly makes DOCS a company with global reach and personal focus. Our History: DOCS was formed in The Netherlands in 1997 and grew to become the premier resourcing provider to the European pharmaceutical industry. The company was acquired by ICON plc in 2007 and was merged with ICON’s existing resourcing division, ICON Contracting Solutions. The merged company is now known as DOCS, and offers clients over 15 years of experience in the provision of global resourcing solutions. For more information, please visit www.docsglobal.com& www.iconplc.com.
    公司主頁
    少妇AV射精精品蜜桃专区| 成全电影大全在线观看国语| 国产精品夜间视频香蕉| 色噜噜狠狠狠狠色综合久一| 青柠影院在线观看免费高清电视剧| 久久亚洲国产精品123区| 日韩 中文在线| 99riva一区二区在线观看| 日韩人妻一区二区三区蜜桃视频| 中文字幕无码人妻视频|