Providence Clinical Research (PCR) promotes the highest quality clinical research in the community setting. We are a "Special Populations" Contract Research Organization with a full service, independent research center. Our expertise spans across all phases of regulated development. We also work closely with our regional medical community to cultivate a progressive community-based research enterprise. For this we provide support, training, oversight and tools to ensure the success of established and new clinical investigators and investigative sites. We advocate for study subjects, maintain the highest professional standards, and exemplify investigative site excellence. Providence Clinical Research (PCR) exists to meet the needs of sponsors, community-based investigators and study subjects to optimize the safe, efficient and timely conduct of high quality clinical research in the community setting. In the spirit of the FDAs Critical Path Initiative and the NIH Roadmap: Reengineering the Clinical Research Enterprise, Providence Clinical Research provides critical standards-based and performance-based services are streamlined performance of clinical research services, with rapid regulatory submissions, rapid contract review and approval, rapid initiation, rapid enrollment, excellent recruitment, and responsive staff , eClinical technology , investigator support services (i.e., certified CRCs, study procurement, contracts and budget negotiation and administration, IRB submissions, regulatory updates, adverse event reporting assistance, study document management and clinical trial management tools including state of the art eClinical technologies) , training, certification and continuing education programs.
The following is the list of scholars from Provident Clinical Research who contributed and/or serves as editors for one or more OMICS International journals and conferences