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更新于 5月22日

區(qū)域合同經(jīng)理 (法律背景)

2-2.5萬(wàn)·13薪
  • 上海浦東新區(qū)
  • 3-5年
  • 碩士
  • 全職
  • 招1人

職位描述

合同審核合同起草臨床試驗(yàn)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(diǎn)

上海浦東新區(qū)晶耀商務(wù)廣場(chǎng)-1座

職位發(fā)布者

姜女士/招聘經(jīng)理

剛剛活躍
立即溝通
公司Logo艾昆緯醫(yī)藥科技(上海)有限公司
IQVIA(紐交所代碼:IQV)是全球?qū)W⑸茖W(xué)領(lǐng)域的高階分析、技術(shù)解決方案和臨床研究服務(wù)供應(yīng)商。IQVIA利用深入分析、前沿技術(shù)、大數(shù)據(jù)資源和廣泛領(lǐng)域的專(zhuān)業(yè)知識(shí),智能連接醫(yī)療生態(tài)的各個(gè)環(huán)節(jié)。IQVIA Connected Intelligence?快速敏銳地為客戶提供強(qiáng)大的數(shù)據(jù)洞察,幫助客戶加速創(chuàng)新醫(yī)療的臨床開(kāi)發(fā)和商業(yè)化進(jìn)程,以更好的醫(yī)療成果惠及患者。IQVIA擁有約72,000名員工,足跡遍布100多個(gè)國(guó)家/地區(qū)。IQVIA擁有多元化的加強(qiáng)型隱私技術(shù)和保障手段,能夠在保護(hù)個(gè)人隱私的同時(shí)對(duì)信息進(jìn)行管理和分析,幫助醫(yī)療利益相關(guān)方有效開(kāi)展精準(zhǔn)療法,獲得更佳的療效。這些洞見(jiàn)和能力能夠幫助生物科技、醫(yī)療器械、制藥公司、醫(yī)學(xué)研究者、政府機(jī)關(guān)、支付方以及其他醫(yī)療利益相關(guān)方,獲得對(duì)疾病、人類(lèi)行為和科技進(jìn)步更深入的理解,共同朝著治愈各類(lèi)疾病的方向邁進(jìn)。
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