• 5-7年经验
  • 硕士
  • 招1人
  • 11-09 发布
  • 五险一金
  • 员工旅游
  • 交通补贴
  • 餐饮补贴
  • 绩效奖金
  • 定期体检

职位描述

职位描述: 1、 Education:√Doctor√Master2、 Experience:At least 3 years of clinical research experience and at least 2 years of clinical project management experience; Global trial experience is preferred3、 Language Skills:English is working language4、 professional knowledge& Skills:Education background is life science related and medical training is preferred; Project management certification is preferred5、other requirements: Be able to manage long term oversea travel position statement1、Project Administration - Acts as a primary liaison between the Company and the Customer to ensure study launch, conduct, and closeout according to the Customer’s and the Company's contractual agreement.2、Coordinates project organization, implementation, and management activities between all Company operations and the client. Manages the executed contract and financial aspects of assigned projects, including reviewing study budgets and expenses. Oversees and tracks site payment issues as required. Alerts Finance on the need for Customer invoicing.3、Oversees the regulatory document collection and submission process. Ensures project documentation, including Trial Master Files are complete and audit ready.Assists in the negotiation and contracting process with outside vendors (labs, printers, etc). May perform or oversee site feasibility assessments. Develops and maintains project plans for the study in accordance with Standard Operating Procedures (SOPs) and Work Instructions (WI).4、Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools. Produces and distributes status, resourcing, and tracking reports, and functional area plan to appropriate team members and senior management. Performs ongoing review of project financial status of studies. Alerts senior management to potential issues and ensures necessary corrective action is taken.5、Communication – Be able to prepare and present study material at client meetings and communicates outcomes to project team at review meetings. Attends clinical monitoring staff meetings, project team meetings, clinical committees, and clinical training sessions according to the project communication, project management, monitoring, and/or training plans. 职能类别: 生物工程/生物制药

联系方式

苏州工业园区星湖街218号生物纳米园C14幢4楼

公司信息

天演药业(苏州)有限公司是一家致力于原创性抗体技术及其产品线开发的生物制药公司。公司成立于2012年2月,位于苏州市生物纳米园内。目前拥有研发场地2246平方米,员工125人,其成员毕业于芝加哥大学、加州理工学院、耶鲁大学、洛斯阿拉莫斯国家实验室、法国巴黎大学、瑞士苏黎世理工学院、北京大学、中国科学院等国际顶尖学府。天演药业将信息技术与生物技术完美结合,开发出了具有独立自主知识产权的动态精准抗体技术,并运用此技术,开发出针对特定肿瘤靶标的治疗性及诊断用的单、双特异性抗体药物,同时专注于单、双特异性抗体的产品开发与合作。2015年天演药业完成B轮融资,顺利完成了与多家国内外知名药企的项目合作,并致力于打造自己的创新产品线。天演药业已建立了世界近万亿级的可开发性抗体库,世界构建了无缝整合噬菌体和酵母的筛选平台。能精准地设计、构建及筛选治疗性抗体,并能生成针对不同靶点的单特异与双特异性抗体,并且这些抗体具有特别优异的靶点交叉性,使得产品更加快速地鉴定体内和体外的药效及安全性,加速产品的临床研发。目前公司正在快速发展之中,真诚的邀请具有前瞻力、领导力、独立思考能力以及希望在全新的结合了信息与生物技术的创新公司做出一番事业的有志之士加入我们,天演将以广阔的发展平台、优厚的薪酬福利虚位以待。

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