南京招聘

? In general provide internal support to the Clinical Logistics Operation Leader as a project resource supporting internal systems and systems set-up but also executing day-to-day data analysis of the operational and financial study status (planned versus current) and reporting activities.
? Prepare draft logistics description including all sub plans and other mandatory documents as applicable
? Review Central Files Maintenance Plan (CFMP) and set up of CTSL filing structure in co-operation with Clinical Logistics Operation Leader and Project Leader. Support implementation according to the CFMP and oversee CTS&L quality checks according to the plan.
? Review SOP list under direction of the Clinical Logistics Operations Leader
? In case of standalone studies drafts all required documents (SOP-List, CFMP, eg.)
? Initiate, set-up and maintain Management Systems on a regular basis
? Develop project specific or prepare standard Client Reports format using standard reports where possible and required. May be involved with ad hoc client requests for reporting.
? Arrange project related training for project team members and new team members under the
direction of the Clinical Logistics Operations Leader if applicable
? Attend project specific training, as required
? Attend project meetings as required per SOPs and Work Instructions
? Support Clinical Logistics Operations Leader in identifying, implementing, reviewing and up-dating project specific operational and financial performance metrics (e.g. PO report, Time reports)
? As required support Clinical Logistics Operations Leader in managing internal procurement process, ensuring that appropriate Scope of Work documents and Purchase Requisitions are in place
? Conduct project close out in management systems at end of project.
? Support projects audits.
? Support Clinical Logistics Operations Leader in invoice review.
? Complete routine administrative tasks in a timely manner (e.g. timesheets, metrics)
*Job Qualifications
Skills
Excellent interpersonal, verbal and written communication skills
? Client focused approach to work
? A flexible attitude with respect to work assignments and new learning
? Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
? Willingness to work in a matrix environment and to value the importance of teamwork.
? Proficient in use of web based IT systems and MS Excel, PowerPoint and Word.
? Analytical mind with attention to detail.
? Result and solution oriented

Education
? Preferred a Bachelor’s degree or equivalent in a science related field, with an advanced degree desirable
? or sufficient, relevant job experience
? or another relevant education

Language Skills
? Proficient in local language and profound working knowledge of the English language

Minimum Work Experience

? Proven relevant experience in healthcare, clinical research, logistics, project management or contract research organization.

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。