Clinical Research Central Office

UWCCC临床研究中心办公室(CRCO)提供基础设施来支持临床 UWCCC调查人员的研究。CRCO由经验丰富的研究人员组成，他们是 生物统计共享资源和癌症信息学共享资源为这方面的支持提供了便利。 提供的服务包括： 协议审查和执行，包括协议识别、协议审查、协议 激活、研究关闭、数据库管理。 人类科目委员会的协调和监督，包括启动和继续执行议定书 年度审查。 集中化的患者跟踪。。 研究政策的制定、协调和执行，这是制定和实施的 通过项目经理委员会和制定标准作业程序。 培训协调与实施。 促进教育和纠正行动。 行政监督。 为UWCCC调查员发起的研究提供的其他服务包括： 方案开发和患者病例报告表开发， 数据摘要和最终报告表。 CRCO由副主任(H Bailey)和临床助理主任监督 研究(R.Arzoomania)，在临床研究方面合作了17年以上。

The UWCCC Clinical Research Central Offices (CRCO) provides the infrastructure to support the clinical research of UWCCC investigators. The CRCO is composed of experienced research staff and they are facilitated in this support by the Biostatistics Shared Resource and the Cancer Informatics Shared Resource. The services provided include: Protocol review and implementation, which includes protocol identification, protocol review, protocol activation, study closure, database management. Human subjects committee coordination and oversight, which includes protocol activation and continuing annual review. Centralized patient tracking. . Research policy development, coordination and implementation, which is developed and implemented through the Program Manager Committee and the development of standard operating procedures. Training coordination and implementation. Education and corrective action facilitation. Administrative oversight. Additional services available to UWCCC investigator initiated studies include: Protocol development and patient case report form development, Data abstraction and final report tables. The CRCO is under the supervision of the Associate Director (H Bailey) and Assistant Director for Clinical Research (R. Arzoomanian), who have collaborated on clinical research for over 17 years.