Office for Clinical Research

弗吉尼亚大学（UVA）癌症中心临床研究办公室（OCR）的总体目标 提供中央临床研究基础设施，以便： 促进临床研究的启动和管理 协助癌症中心的主要研究者和临床医生进行患者的筛选和入组 临床研究 监测临床试验与方案相关的所有监管方面的合规性 审查委员会、IRB、州和联邦指南 为所有参与临床研究的癌症中心工作人员提供培训和教育计划 研究 为内部和外部质量保证审计提供支持 将临床研究的可用性传达给癌症中心的医生， 医生和社区 推荐、开发、实施和维护最先进的信息系统，以支持 癌症临床研究的工作流程、数据共享、分析和报告要求 <$培训用户使用Forte Research Systems、OnCore <$临床研究管理系统

The overall objectives of the University of Virginia (UVA) Cancer Center's Office of Clinical Research (OCR) are to provide a central clinical research infrastructure to: ¿ Facilitate the activation and administration of research clinical studies ¿ Assist Cancer Center Principal Investigators and clinicians in the screening and enrolling of patients on clinical research studies ¿ Monitor compliance with all regulatory aspects of clinical trials in conjunction with the Protocol Review Committee, IRB, state, and federal guidelines ¿ Provide a training and education program for all Cancer Center staff involved in clinical research studies ¿ Provide support for internal and external quality assurance audits ¿ Communicate the availability of clinical research studies to Cancer Center physicians, referring physicians, and the community ¿ Recommend, develop, implement, and maintain state-of-the-art information systems to support the workflow, data sharing, analyses, and reporting requirements of cancer clinical research studies ¿ Train users on the Forte Research Systems, OnCore¿ clinical research management system