北京招聘

Results Orientation/ Project Execution-Oversees the logistics aspect of designated projects to ensure that the right supplies are delivered to the right locations at the right time and right conditions-Provides support for development of project specific logistics strategy-Executes clinical logistics procedures for clinical trials-Supports set-up of clinical trial logistics (e.g. kit design & lab material sourcing-Manages and oversees lab kit manufacturing-Prepares and ensures distribution of study documents and materials-Performs day-to-day communication with the clinical team, sites and vendors-Participates in regular study team, as required-Tracks and reports logistics study metrics to the project team-Supports financial control; tracks, checks and compiles invoices-Contributes to meeting study timelines and works efficient with systems in place-Supports toward and ensures he/she stays within budget/time allocated, in agreement with the applicable Laboratory Logistics Services Manager and Laboratory Logistics Coordinator-Supervises transportation, import and export of biological samples in cooperation with investigators, GTC, LLAs, CRAs, laboratories and courier service providers-Manages collection and analysis of laboratory samples for clinical trials-Performs laboratory data management and reporting of lab results to sites-Performs query managementDomain Expertise-Supports central filing and final archiving activities.Skills: ·Understanding of the regulatory framework of Clinical Trial Supplies·Multi-tasking and prioritization ability·Result-oriented, confident, self-motivated, and driven/high energy·Credible team player with good facilitation skills·Good interpersonal , verbal and written communication skills·Solid communication (verbal & written) and negotiation skills. ·Ability to influence and gain collaboration from and respect of key stakeholders·Demonstrated ability to conduct business in English (written and spoken) and in local language if different from English·Good knowledge of Microsoft Office programs (Word, PowerPoint and Excel)·Strong client focus·Ability to build rapport with a culturally diverse group at multiple levels and disciplines·Flexible, capable of managing change and ambiguity·Good analytical capabilities combined with creative problem-solving skills and a sense of urgency

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。