Support of NCI CCR Clinical Research and Bioinformatics

该计划涉及为NCI癌症研究中心(CCR)提供信息技术支持的许多方面。我们开发和/或维护的项目包括：1)LabMatrix，这是一个组织研究和库存系统，用于管理组织的收集和存储，以及这些组织的研究分析产生的数据。2)IRIS，用于所有CCR人类和动物协议以及DCEG特别研究IRB管理协议的协议生命周期管理系统。3)CCR协议视图，NCI和NIH临床中心分发我们的临床试验协议的网站。4)合流维基，便于CCR科学和管理人员的标准化文档、协作和简单的网站开发。汇流作为我们的DB Quick技术的接口，允许超快开发简单的基于Web的数据库应用程序。5)JIRA问题管理软件，用于支持CCR中需要管理用户请求的小组。6)未来研究员，这是一个收集和审查潜在博士后研究员提交的简历的网络应用程序。7)预算管理系统，用于向CCR主要研究人员和核心研究小组分配资金。8)将CCR网站重新设计和重新设计为以Drupal为基础的网站。9)CCR转诊。这提供了一种标准化的方式来管理潜在的临床试验参与者及其医疗信息，因为它与有资格参与CCR临床试验有关。10)PA Tracker，用于跟踪整个审批过程中的人力资源包。11)为科学报告提供视频会议支持，包括CCR大型会议和著名讲座系列，以及许多较小的科学合作项目。11)CCR管理网站的第508条合规性。12)Scribe，一种直接从研究对象收集研究数据并让这些数据经过实时验证并输入研究人员数据收集系统的方法。

This program is involved in many aspects of information technology support for the NCI Center for Cancer Research (CCR). Projects which we develop and/or maintain include the following: 1) Labmatrix, a tissue research and inventory system for managing both the collection and storage of tissues, as well as data resulting from the research analysis of these tissues. 2) iRIS, a protocol lifecycle management system used for all CCR human and animal protocols as well as DCEG Special Studies IRB-managed protocols. 3) CCR Protocol View, a website for NCI and NIH Clinical Center distribution of our clinical trials protocols. 4) Confluence wiki, which facilitates standardized documentation, collaboration, and simple website development for CCR scientific and administrative staff. Confluence acts as an interface to our DB Quick technology, allowing ultra fast development of simple web-based database applications. 5) JIRA issue management software, used to support those groups in the CCR that need to manage user requests. 6) Future Fellows, a web application for the collection and review of C.V.s submitted by potential postdoctoral fellows. 7) Budget Management System, used to allocate funds to CCR principal investigators and core research groups. 8) Redesign and reengineering of the CCR website to a Drupal-based site. 9) CCR Referrals. This provides a standardized way to manage potential clinical trial participants and their medical information as it pertains to being qualified to participate in CCR clinical trials. 10) PA Tracker for the tracking of human resource packages through the approval process. 11) Video conference support for scientific presentations, including the CCR Grand Rounds and Eminent Lecture series, as well as many smaller scientific collaborations. 11) Section 508 compliance of CCR-managed websites. 12) Scribe, a method of collecting study data directly from study subjects and having that data go through real-time validation and entry into a researcher's data collection system.