北京招聘

Essential Function
The Proposal Developer's role is to create budgets and other components for proposals across all product areas within PAREXEL Informatics
Key Accountabilities
? Create proposal, including budgets and budget grids, task and responsibility tables, timetables, description of services and payment schedules.

Proposal Development
? Participate in proposal development team (PDT) meetings to:
o Identify issues and client requirements
o Identify key team members
o Recommend internal resourcing and pricing
o Establish agreement on timelines and deliverables from the PDT meeting, and follow-up to ensure adherence
? Create accurate budget which reflects both Perceptive and client needs assuring accuracy, consistency and competitiveness
? Ensure appropriate and accurate mapping to client budget specifications
? Provide quality deliverable to agreed deadlines

Other Tasks
? Processes and maintains information relating to proposal documents in relevant databases (primarily CRM and PERFORM)
? Participates in the development and testing of tools and procedures
*Job Qualifications
? Well organized with good oral and written communication skills
? Strong ability to manage multiple projects
? Good numeracy skills
? Good analytical and problem-solving skills
? Comprehensive knowledge of relevant software (Windows, Word, Excel, Outlook, Databases)
? Knowledge of clinical trials and the pharmaceutical industry a plus

Education
? Bachelors Degree in Life Science, Business or equivalent

Language Skills
? Fluent in English, oral and written
? Knowledge/fluency in an additional language a plus

Minimum Work Experience
? Minimum of three years previous experience in Clinical Data Management, proposal development, marketing, operations, technology or clinical research a plus

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。