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上海-徐汇区 1-3年 本科
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Talent Acquisition Manager · 利洁时(中国)投资有限公司
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职位介绍
职责描述: This is a role within the Clinical Operations team to meet business objectives through insight into Reckitt products from available data, sound oversight of clinical study activities and the generation of robust clinical study evidence. INSIGHT •Utilise clinical study data from previous studies for strategic use. •Give valid interpretations and any limitations from past data. •Assist in giving expert operational advice (e.g. innovative approaches such as methods, models and techniques to achieve claims and endpoints) on more complex clinical topics. •Gain strategic awareness about projects related to assigned clinical studies. EVIDENCE Act as a clinical representative: •Lead the study teams for assigned clinical studies in a matrix structure building effective relationships with study teams, ensuring agreed timelines are met. •Attend the Scientific Review Committee meetings and high-level strategy meetings for the assigned clinical studies. •Contribute into the evaluation of probability of success and potential risks when clinical studies are being planned against business objectives. Perform day-to-day activities: •Ensure appropriate assessment, selection and management of vendors for outsourced activities. •Contribute to contract negotiations with vendors. •Ensure the clinical elements of vendor standard operating procedures are in place and meet local, global and Reckitt requirements. •Ensure the external vendor staff are sufficiently trained and experienced to conduct each specific clinical activity. •Manage and oversee clinical studies (IMP, device, cosmetics) of low to normal complexity/single country. •Assist in managing and overseeing clinical studies of high complexity/multiple regions. •Ensure study designs and endpoints for planned clinical studies are in line with the required standards (i.e. ICH-GCP, ISO, any local regulatory standards) and are optimal for meeting the study objectives. •Author or review Protocols. •Author or review various other study related documentation. •Author or review Clinical Study Reports. •Manage and adhere to agreed timelines for studies. •Manage applicable (vendor) contracts. •Manage payments to vendors and manage study budgets. •Support the development of slide sets, reports and publications (abstracts, posters, manuscripts) for internal and external communication of study results. OVERSIGHT Compliance and adherence to SOPs: •Ensure that clinical activities are performed to the required standards (i.e. ICH-GCP, ISO, any local regulatory standards) and ready for inspection. •Input into and adhere to the clinical standard operating procedures. Governance of vendors: •In collaboration with Outsourcing Manager: •Optimize outsourcing of health outcomes activities considering costs, quality and time constraints. 任职要求: •At least 2-3 years (Master’s degree) or 3-4 years (Bachelor’s degree) of clinical operations experience preferably in a clinical or medical department in pharmaceutical/consumer healthcare/cosmetic industry or at a CRO or clinical vendor. •In depth and up to date knowledge of GCP/regulatory standards. •Strong understanding of corporate and operational business needs. •Project management and organisational skills. •Computer literacy (Advanced Microsoft Skills).
其他信息
所属部门:R&D

公司简介

利洁时是一家有着200多年悠久历史的全球消费品公司,创建于19世纪初期,全球总部位于英国。如今的利洁时已经成为一家多元化发展的跨国公司,在全球68个国家和地区拥有40000多名员工。每一天,利洁时有3000多万件产品被送达190多个国家的顾客手中。 利洁时与世界各地的伙伴紧密合作,为消费者带来备受信赖和推崇的产品,旗下拥有众多市场高度认同的卫生、健康和营养产品品牌,包括杜蕾斯、滴露、益节、亮碟、薇婷等。 利洁时的产品于1916年登陆中国,迄今已经100多年。利洁时致力于深耕中国,长期投资,鼓励本地研发和创新,提高中国消费者的生活水平。 利洁时通过卫生防护、健康疗护、营养守护,致力于打造一个更洁净、更健康的世界,让人们平等地享有高品质的卫生、健康和营养。
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