南京招聘

Position Summary

· Support project team to provide administrative, technical and logistical supports to ensure timely and efficient execution of clinical trials, and in accordance with ICH-GCP, regulatory requirements and the SOPs/WI/IG of dMed.

· Provide the appropriate administration support at the function level.

Key Responsibilities

Study Support

l  Request and track payments for study related cost

l  Update study information using proper tool

l  Support Project Manager (PM) for study documents archiving

l  Attend appropriate training and meeting as applicable

l  Maintain and develop study tracking and provides analysis report to Project Manager

l  Support Project Manager on study budget control by timely tracking, reporting of actual cost and forecast drafting, and expense reconciliation

Other responsibilities

l  Provide appropriate the administration support at the function level including but not limit to org-chart maintenance & update, coordination of function meeting, training and other activities.

l  Take the function coordinator to support the implementation of company policy and HR requirements etc.

l  Support BD activities including but not limit to prepare quotation, visit client and communicate with other function or client.

l  Complete other tasks assigned by line manager

Education and Key Competency Requirements

    

• Bachelor degree preferred
• Solid proficiency in Microsoft Word, Excel, PPT
• Experience in clinical trial administration preferred
• Detail oriented, and focus on quality and efficiency
• Communicate effectively and appropriately with internal & external team including vendors and clients
• Strong customer service orientation
• Work with project teams to identify and articulate complex problems
• Effective interpersonal skills and collaborative team player
• Continuous learning capability

全球知名生物医药企业资深研发团队打造的创新服务公司。让你的职场起点更高，更充满挑战和精彩。
 
我们是谁？
 
    基于中国面向全球制药，生物技术和医疗器械公司的临床开发服务和解决方案提供商:
· 临床试验全程及专业领域服务：临床试验设计、数据管理及系统开发、生物统计及编程、运营和项目管理、报告撰写、注册运作和策略、质量保证和稽查、药物安全警戒和风险管理
· 战略咨询服务：临床开发和注册策略、研发功能和架构设计、技术支持和国际化支持。
 
为什么选择我们？
 
· 缔脉定位于以高品质服务和专业精神成为业界典范。
· 缔脉管理层在中国生物医药研发领域耕耘十多年培养了1000+优秀人才。
· 缔脉致力于通过系统培训，研发实践和开放式文化培养新一代生物药物研发国际化人才。
 
创始人及部分核心专业领域


创始人 - 谭凌实博士：拥有20多年跨国一流制药公司总部高级管理经验。此前担任辉瑞公司全球药物开发运营副总裁，在中国成功创建了首屈一指的研发中心，且经历10多年发展壮大到多个地点，成为辉瑞全球核心的研发中心之一，承担药物临床开发、安全风险管理、注册、临床稽查等关键职能。谭博士多年为RDPAD, DIA 的核心成员，担任重要职务,包括研发委员会主席, 全球董事等。谭博士还带头建立了与国内一流高校的教育培训合作，比如复旦大学、北京大学，交通大学。培养了不少拥有专业技能和行业知识的临床数据管理和编程人才。谭博士有在美国建立初创企业的经验，且在美国一流制药企业研发中心工作多年。谭博士拥有生物统计博士学位。