成都招聘

职位描述：
Job Description :
 
- Ensures delivery of PAREXEL Informatics RTSM products and services to clients within expected timelines and budget with quality, including resource planning and management
- Provide overall project leadership during the build phase and/or after go-live
- Is key client contact for the study and manages the client relationship
- Actively identifies , manages, and mitigates any project risks, including ensuring appropriate input from all stakeholders, maintaining accurate documentation, and communicating to internal and external parties as appropriate
- Collects client requirements and produces the Specification and prototype based on the proposal, protocol and specific project needs
- Responsible for all build tasks
- Lead User Acceptance Testing
- Facilitates training for clients as required
- Attends face to face client meetings and investigator meetings as necessary (may require travel)


Job Qualifications :
 
Minimum Work Experience:
-Relevant work experience preferred, including but not limited to: Either Clinical Trial or IT experience e.g.Database designer/programmer; Related environment working with IVR/IWR system;working in a clinical trials environment or client facing experience e.g. managing live studies or equivalent.

Skill:
-Excellent customer service skills
-High attention to detail
-Ability to work independently and in a team environment
-Excellent verbal and written communication skills
-A flexible attitude with respect to work assignments and new learning.
-Ability to manage multiple and varied tasks with enthusiasm and prioritize workload
-Problem resolution skills; ability to analyze and solve a range of simple and complex problems
-Good computer skills
-Demonstrates initiative and innovation

Language:
-Fluent in verbal and written English 举报 分享

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。