Clinical Research Central Office

UWCCC临床研究中心办公室（CRCO）提供支持临床研究的基础设施。 UWCCC研究人员的研究。CRCO由经验丰富的研究人员组成，他们 在生物统计学共享资源和癌症信息学共享资源的支持下， 所提供的服务包括： 方案审查和实施，包括方案识别、方案审查、方案 激活、研究关闭、数据库管理。 人类受试者委员会协调和监督，包括方案激活和持续 年度回顾。 集中患者跟踪。. 研究政策的制定、协调和执行， 通过项目经理委员会和标准操作程序的发展。 培训协调和执行。 促进教育和纠正行动。 行政监督。 UWCCC研究者发起的研究可获得的其他服务包括： 方案制定和患者病例报告表制定， 数据提取和最终报告表。 CRCO由副主任（H Bailey）和临床助理主任监督 研究（R. Arzoomanian），他们在临床研究方面合作超过17年。

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.