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    更新于 8月5日

    區域合同經理 (法律背景)

    3-3.5萬·13薪
    • 深圳福田區
    • 5-10年
    • 碩士
    • 全職
    • 招1人

    職位描述

    合同審核合同起草臨床試驗臨床研究合同審查
    ● Services rendered will adhere to applicable client's SOPs, WIs, policies,
    local regulatory requirements, etc.
    ● Support creation and maintenance of contract templates in accordance with
    changes in laws, regulations, or corporate policies.
    ● Support creation and maintenance of fallback language and negotiation
    guidelines related to contract templates.
    ● Support training on contract templates and fallback language and provide
    training to first line negotiators and others as required.
    ● Provide specialized support and guidance on the negotiation of CTAs and CDAs
    to first line negotiators.
    ● Work with the legal department to create risk assessments to support the
    decision-making process.
    ● Assess risks of legal terms and conditions independently and communicate
    them to stakeholders such as clinical team, law department, and internal team
    where appropriate. Provide guidance to 1st line negotiators, stakeholders and
    others as required.
    ● Lead negotiations on Master Agreements and custom templates or those
    requiring extensive modifications and identify potential risks to the business.
    ● Participate in contract negotiations on terms and conditions of high-risk
    and complex agreements and other relevant legal documents as they relate to
    clinical trials and company/departmental policies (subject to and within the
    limits of the client's negotiation parameters and the client's form of written
    contract). For the avoidance of doubt, the service shall not have authority to
    sign contracts on behalf of the client's party.
    ● Coordinate with cross-functional departments to ensure consistency and
    compliance with process, external communications and policies.
    ● Assist in coaching/mentoring staff members.
    ● Liaise with all members of clinical team as needed in addition to
    representatives of investigator sites, academic research organizations,
    contract research organization, and site management organizations as directed.
    ● Identify and promote best practices. Adhere to SOPs, ethics and departmental
    compliance as determined by GCDO management as well as R&D companies,
    corporate, HCC and QA guidelines.
    ● Collaborate with internal stakeholders to ensure proper dissemination and
    management of knowledge.
    ● Monitor departmental processes to ensure compliance with corporate policies.

    工作地點

    深圳福田區市中心區

    職位發布者

    姜女士/招聘經理

    昨日活躍
    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。
    公司主頁
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