南京招聘

Primary Responsibilities

Maintain local documentation as required by legislation (including archiving/tracking/retrieval)

Support the submission and distribution of reports and relevant tracking

Support distribution and tracking of distribution of FU letters

Support inspection preparedness activities

Consistently apply case receipt policies and practices as per Company SOP

Consistently apply archiving policies as per Company SOP

Technical Skill Requirements

Demonstrated computer literacy, particularly in the use and management of relational databases

IT skills (Word / Excel)

Qualifications (i.e., preferred education, experience, attributes)

High School Diploma required

Ability, with supervision, to solve routine problems and to surface issues constructively

Ability to make basic decisions with an understanding of the consequences

Ability to achieve personal objectives while meeting departmental standards of performance

Ability to work under supervision in a matrix organization

High attention to detail

High interpersonal skills

Fluency in spoken and written English

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。