Support of NCI CCR Clinical Research and Bioinformatics

该计划涉及NCI癌症研究中心（CCR）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，一个组织研究和库存系统，用于管理组织的收集和储存，以及这些组织的研究分析产生的数据。2)iRIS，一种用于所有CCR人类和动物方案以及DCEG特殊研究IRB管理方案的方案生命周期管理系统。3)CCR Protocol View是NCI和NIH临床中心发布临床试验方案的网站。4)Confluence wiki，为CCR科学和管理人员提供标准化文档、协作和简单的网站开发。Confluence作为DB Quick技术的接口，允许超快速地开发简单的基于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组。6)Future Fellows，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主要研究者和核心研究小组分配资金。8)重新设计和改造社区协调员网站，使之成为一个Drupal网站。9)CCR参考文献。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，因为它与参与CCR临床试验的资格有关。10)PA Tracker用于在整个审批流程中跟踪人力资源包。11)为科学演示提供视频会议支持，包括CCR大型圆桌会议和杰出演讲系列，以及许多小型科学合作。11)第508节CCR管理的网站的合规性。12)Scribe，一种直接从研究对象收集研究数据的方法，并将该数据进行实时验证并输入研究人员的数据收集系统。

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.