PCIRC

这个子项目是许多利用资源的研究子项目之一 由NIH/NCRR资助的中心拨款提供。子项目的主要支持 而子项目的主要调查员可能是由其他来源提供的， 包括其它NIH来源。 列出的子项目总成本可能 代表子项目使用的中心基础设施的估计数量， 而不是由NCRR赠款提供给子项目或子项目工作人员的直接资金。 参与者和临床互动资源核心（PCIRC）： 参与者和临床互动资源关键职能的总体目标是促进波多黎各联盟成员机构当前基础和临床研究活动向波多黎各临床转化研究联盟新范式的转变。其主要使命是通过确保安全和具有成本效益的研究所需的人员、设施和资源的可用性，培养和促进参与临床和转化研究的环境。 这一关键职能旨在： 1.通过联盟成员机构维持和扩大现有的以门诊为基础的临床研究设施，并开发潜在的住院和社区外展站点，以进行转化临床研究。 2.开发现有资源，用于招募研究参与者参与协议，这可能会影响社区对特定健康问题的认识，重点是西班牙裔健康差异。 3.在社区和研究人员之间建立联盟，以促进公众的信任和参与，并为代表性不足的领域（例如，农村地区）。 4.实施机制，促进基础、临床和流行病学资源的互动和协作。 5.加快研究者启动方案。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Participant and Clinical Interactions Resources Core (PCIRC): The overall goal of the Participant and Clinical Interaction Resources key function is to contribute to the transformation of current basic and clinical research activities at Consortium-member institutions in Puerto Rico to the new paradigm of the Puerto Rico Clinical Translational Research Consortium. Its primary mission will be to foster and promote an environment of participation in clinical and translational research by assuring the availability of personnel, facilities and resources for safe and cost-effective research. This key function aims to: 1. Maintain and expand the current outpatient-based clinical research facilities available through Consortium-member institutions and develop potential inpatient and community outreach sites for the conduction of translational clinical research. 2. Develop current resources for the recruitment of research participants in protocols, which may influence the community awareness on specific health issues with emphasis on Hispanic health disparities. 3. Build an alliance between communities and researchers that will foster public trust and engagement and create opportunities for research in under-represented areas (e.g., rural areas). 4. Implement mechanisms to foster the interaction and collaboration of basic, clinical and epidemiological resources. 5. Expedite initiation of protocols by investigators.