南京招聘

职位描述：
At PAREXEL, we believe that the power to work independently and intelligently should be yours every day.
Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world. Be part of our empowered PAREXEL Statistical Programming team and contribute to our high performance approach.
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An exciting and rewarding opportunity has arisen to join our international team as a
PRINCIPAL STATISTICAL PROGRAMMER
to contribute to meaningful advances that benefit patients in need.
As a Principal Statistical Programmer you will be recognized as a subject matter expert, providing technical support and expert advice to internal and external sponsors. PAREXEL will provide you with the perfect opportunity to expand on your experiences and develop new skills in a stimulating work environment
KEY RESPONSIBILITIES include:
? Ability to fill Primary Statistical Programmer role on projects. The Primary Statistical Programmer will:
o Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to.
o Coordinate and lead a statistical programming team to successful completion of a study within given timelines and budget.
o Monitor project resourcing, project budgets, and identify changes in scope.
? Provide a broad range of leadership and influencing capabilities to achieve the business objectives and goals for both PAREXEL and sponsors.
? Provide oversight and guidance on multiple-trial programs, complex trials, and submission projects (including Integrated Summaries of Safety/Efficacy).
? Proactively participate in and/or lead process/quality improvement initiatives.
*Job Qualifications
KEY SKILLS include:
? Extensive knowledge and understanding of the programming and reporting process.
? Ability to learn new systems and function in an evolving technical environment
? Ability to successfully work together with a (“virtual”) team (including international teams as required) as well as independently.
? Strong project management skills.
? Show commitment to and perform consistently high quality work

Starting your journey with PAREXEL comes along with an extensive induction program and ongoing training while following your individual career path. We have been recognized as a 2015 “Training Top 125” by Training Magazine for our excellence in employer-sponsored training and development programs.
On your PAREXEL journey, you will be involved in database programming efforts related to medical coding for clinical trials, you will work in cross-functional teams, and with managers who know your strengths. If you’re looking for flexibility and work-life balance, we’re here to listen and help you move forward with your individual career path.
There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. If you’re looking to collaborate with life science industry leaders, gain exposure to industry changing technology, and find the security of a role within a global CRO join a team that will help you move forward with your individual career path. 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。