南京招聘

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs.

Statistical Trial Analysis
* Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans.
* Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, and conducting the actual analysis once a reporting database is created.
* Collaborate with data management in the planning and implementation of data quality assurance plans.
* Maintain proficiency with respect to SAS programming and statistical methodology and in applying new and varied methods.
* Effectively justify methods selected and implement previously outlined analysis plans.
* Conduct peer-review of work products from statistical colleagues.
* Effectively utilize current technologies and available tools for conducting the clinical trial analysis.

Communication of Results and Inferences
* Collaborate with other statistical colleagues to write reports and communicate results.
* Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.
* Assist or respond to regulatory queries working in collaboration with other statistical colleagues.

Therapeutic Area and Systems Knowledge
* Understand relevant disease states in order to enhance the level of customer focus and collaboration.
* Ensure replication of tools and systems, where applicable and stay informed of technology advances.

Regulatory Compliance
* Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes and training.


OTHER INFORMATION
* Proficiency in the SAS programming language
* Interpersonal/teamwork skills for effective interactions
* Technical growth and application with working knowledge of statistics and statistical software
* Self-management skills with a focus on results for timely and accurate completion of competing deliverables
* Creativity and innovation
* Demonstrated problem solving ability and attention to detail
* Data analysis, technology, and systems expertise

华斯泰生命策略研究所（VitalStrategic Research Institute）（以下间称“华斯泰＂)是一所致力于临床II-IV期开发研究，循证医学、流行病学、以及实效临床研究（outcomes research）的新型国际研究机构。除临床研究外，华斯泰还精于医学培训和通讯、医学信息管理、和医药经济学研究。华斯泰推崇循证医学并且同【中国医师协会】共同协办【中国实效研究和循证医学高峰会】年会。从2008年起，华斯泰研究所同【中国心血管医师协会（CCCP）】和【中国内分泌代谢医师协会（CEA）】共同创立了【中国心血管代谢病系列研究（CCMR）】并负责CCMR所有研究项目的具体执行工作。华斯泰同时还同【中国医师协会】协作主办了“心血管代谢疾病协作临床研究委员会”并负责其所有临床研究的执行。华斯泰位于美国费城，在中国设有上海华斯泰医学咨询有限公司，提供研究项目的执行、管理、监查、数据管理和分析、项目报告等全球服务。

目前VSRI的客户和合作者包括各大跨国医药公司和世界知名研究机构。为配合新启动的临床研究项目，我们决定招聘以下工作职位。