RESEARCH DESIGN, BIOSTATISTICS AND CLINICAL RESEARCH ETHICS

这个子项目是许多研究子项目中利用 资源由NIH/NCRR资助的中心拨款提供。子项目和 调查员(PI)可能从NIH的另一个来源获得了主要资金， 并因此可以在其他清晰的条目中表示。列出的机构是 该中心不一定是调查人员的机构。 A.具体目标 研究设计、生物统计学和临床伦理学(DBRE)计划的具体目标是：1)通过加强研究设计、应用适当的生物统计技术以及加强方案的伦理设计和实施，支持临床和转化性研究设计、生物统计分析和临床研究伦理的方方面面；2)通过研讨会、研讨会和个别工作室预备和工作室会议，培训研究人员临床和转化性研究设计、生物统计学和临床研究伦理；以及3)与RTRN的研究设计和生物统计学组成部分互动，开展多站点临床和转化性研究。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. A. Specific Aims Specific aims of the Research Design, Biostatistics and Clinical Ethics (DBRE) Program are: 1) to support all aspects of clinical and translational research design, biostatistical analysis and clinical research ethics by strengthening study designs, applying appropriate biostatistical techniques, and enhancing the ethical design and implementation of protocols, 2) to train investigators in clinical and translational research design, biostatistics, and clinical research ethics through seminars, workshops and individual Studio Prep and Studio sessions, and 3) to interact with the research design and biostatistics components of the RTRN in conducting multi-site clinical and translational research.