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    更新于 12月18日

    Clinical Study Lead

    2.4萬-3萬·14薪
    • 北京朝陽區(qū)
    • 3-5年
    • 碩士
    • 全職
    • 招1人

    職位描述

    臨床試驗生物工程臨床項目管理臨床方案
    Position description:
    1. Responsible for trial design, planning (timeline and budget) and accountable for clinical study projects in China territory of Qiagen organization by coordinating with activities and stakeholders internally and externally.
    2. Ensure compliance to SOPs, GCP policy, and relevant CFDA regulations in the operation of clinical study.
    3. Responsible for tracking of timeline and budget, ensuring complete trial in a timely manner within budget, and raise up potential issues timely, setup internal and external communications for correction, trouble shooting, and prevention plan.
    4. Draft and implement all study associated documentation including ethical application, CFDA files of trial, study protocols, contracts, site files, audit reports, and study reports.
    5. Review all source documentation, monitor reports, site record, and data for accuracy and ensure timely submission and safe storage of all documentation.
    6. Execute site survey/selection, guide lab preparation, instrument/reagent setup, kick-off meeting/training, logistic of consumables supply and inventory in line with regulations.
    7. Lead CRA/CRC (internal and external) to plan site monitoring, and ensure good monitoring quality in terms of documentation, enrollment progress, data records. Lead data specialist for database design, database implementation on site, integrity check planning, and statistic strategy.
    8. Coordinate communications with investigators, and participate discussions with CFDA relevant reviewers / guideline drafter if necessary
    Hiring requirement/preference:
    1. At least 4 years IVD clinical trial related experiences, Pharma trial experiences could be considered as well, better clinical project management roles.
    2. Strong and solid IVD or bio-tech knowledge, medical or clinical lab related backgrounds preferred.
    3. Proficiency of English oral communication, and technical reading and writing.
    4. Excellent knowledge in CFDA regulation, ISO international standards, and relevant clinical trial guidance.
    5. Strong ability in inter-personal skill, project management skill, problem-solving mindset

    工作地點

    太陽宮大廈1103

    職位發(fā)布者

    梁曉霞/人事經理

    昨日活躍
    立即溝通
    公司Logo凱杰企業(yè)管理(上海)有限公司
    ?QIAGEN是一家專業(yè)化致力于生物分子樣品制備解決方案的跨國經營企業(yè),總部位于德國。1984年,QIAGEN在德國成立,1996年在美國紐約納斯達克上市。QIAGEN在全球有亞太、日本、北美、歐洲四個地區(qū)總部,有19個分公司,有近3,000雇員,有超過500個的產品,有超過40萬的用戶,擁有409個已被批準的專利,有300多種專利正在申請之中。是在生命科學研究、應用檢測和臨床診斷等領域的行業(yè)巨頭。作為分子檢測技術領袖,生物分子樣品制備方案的全球主要供應商,QIAGEN-凱杰生物科技可謂名聲赫赫,是大家聽得比較多的名字。許多生物科學家們都對QIAGEN推崇備致,交口稱贊QIAGEN的生物分子分離純化制備技術,無一例外的聲稱自己取得的科研成果都得益于QIAGEN的產品和技術。
    公司主頁
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