南京招聘

The Senior Biostatistician works independently in the production and quality control of analysis plans,
reports, derived datasets, tables, listings and figures, provides statistical advice to clients and fulfills the
project primary role within a designated project team

Key Accountabilities
？？Coordinate and lead a project team to successful completion of a project within given timelines
and budget.
？？Interact with clients as key contact with regard to statistical and contractual issues
？？Perform QC of derived datasets, tables, figures and data listings produced by other members of the
department.
？？Check own work in an ongoing way to ensure first-time quality.
？？Understand and apply advanced statistical methods.
？？Lead production and quality control of randomizations, analysis plans, statistical reports, statistical
sections of integrated clinical reports and other process supporting documents.
？？Provide a supporting role as a non-voting independent statistician providing data and analysis for
DMC review.
？？Support of Business Development, e.g. by actively contributing to study design considerations in
internal and client meetings, providing and discussing sample size scenarios, support of budget and
proposal development, attending and preparing bid defense meetings.
？？Travel to, attend and actively contribute to all kind of client meetings as appropriate (e.g.
discussing analysis concepts, presenting and discussing study results)
？？Additional responsibilities as defined by supervisor/manager.

精鼎医药（Parexel International）是全球领先的药物研究合同委托机构（CRO），总部位于美国生物医药圣地马萨诸塞州的波士顿附近，在世界各地拥有71个办事处，约17,600 名员工，为超过100个国家的客户提供服务。

精鼎医药成立于1982年，在三十多年的历程中，一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商，并且取得了卓越成果。目前，我们能够提供全世界CRO领域全面的新药临床阶段研发服务，服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。

将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案，可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。