Quality Assurance and Reporting

项目总结/摘要 CTSA计划的主要目标是支持研究机构， 提高临床转化研究的效率、有效性和范围。 然而，现实是有行政报告和批准要求 与进行转化研究有关。这些要求包括NCATS Prior 批准主要人员变动、请求结转资金等活动， 标准年度报告和人类受试者事先批准KL 2学者和 试点项目。如果管理报告要求包含错误或不完整 这一过程延迟了临床转化研究的进行。因此， 确保我们的报告质量，以及我们作为一个中心，满足报告 NCATS的期望。 这一行政补充将支持一个工作人员职位， 打算管理和确保报告活动的质量保证， NCATS。该职位将与评价主任、PI/主任和 行政主任确保报告要求前后一致， 高效且无差错。填补工作人员职位的个人将有助于 在我们当地的CTSA中心制定程序，并将分享和 向CTSA网络传播流程和程序效果良好。

Project Summary/Abstract A primary goal of the CTSA Program is to support research institutions to improve the efficiency, effectiveness, and reach of clinical translational research. However, the reality is there are administrative reporting and approval requirements related to conducting translational research. Such requirements include NCATS Prior Approval for activities such as changes in key personnel, requesting carryover funds, standard annual reporting, and human subjects Prior Approval for KL2 Scholars and for Pilot Projects. If administrative reporting requirements contain errors or incomplete material this process delays the conduct of clinical translational research. As such, it is necessary to ensure quality of our reporting and that we, as a hub, meet reporting expectations by NCATS. This administrative supplement will support a staff position with the intention of managing and ensuring quality assurance for reporting activities to NCATS. This position will work with the Director of Evaluation, PI/Director and Administrative Director in ensuring that reporting requirements are consistent, efficient and error free. The individual who fills the staff position will contribute to the development of procedures at our local CTSA hub and will share and disseminate processes and procedures work well to the CTSA network.