天津招聘

Basic function:
1) Provide overall project management, in both the technical and the administrative aspects, of clinical projects in a timely and effective manner and in accordance with GCP.
2) Primarily responsible for liaising with sponsors and leading Company project teams of cross-functional members, which generally include project CRAs, study coordinators, statisticians, data management, regulatory affairs and medical writing personnel.
3) General areas of responsibility include: project assessment and initiation, resource procurement and planning, project implementation, leading and motivating a cross-functional team, milestone planning and tracking, ensuring that projects are progressing according to quality standards, SOPs, ICH and/or other guidelines to fulfill local regulations, production of key project progress reports, oversight of communications between Company and sponsor, and contract and financial management.

Qualification:
1) A bachelor degree (or above) in a life science (preferably paramedical) field.
2) At least 3 years’ work experience in clinical research monitoring.
3) Proficiency in both written and spoken English.
4) Demonstrated understanding of workflow process, and roles and responsibilities of multiple functional areas.
5) Demonstrated ability to understand, explain and communicate project concepts and put into detailed plan.
6) Leadership skills that include the ability to gain trust and confidence with a variety of clients as well as within the company; detail oriented; strong written and oral communications skills, as well as excellent interpersonal skills; motivated to work consistently in a fast-paced and rapidly changing environment.

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。