The PCR Mission Statement  
Mission Statement...

  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 FDA's Critical Path Initiative and the NIH Roadmap: Reengineering the Clinical Research Enterprise (http://nihroadmap.nih.gov), Providence Clinical Research provides critical standards-based and performance-based services:

  • 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 staff at Providence Clinical Research bring extensive, cross-cutting clinical research experience as well as in-depth knowledge of the needs of sponsors, CRAs and investigators. All are dedicated to uncompromised quality, streamlined performance and the highest standards of research. PCR believes that the following criteria are central to the performance of high quality clinical research:

  • Patient safety (good communication and reporting procedures)
  • Attention to detail
  • Clean, quality data on a timely basis
  • Excellent customer service
  • Sensitive to investigator/subject/sponsor needs (good communication)
  • Flexible to change
  • Trained support staff with career paths and low turnover rate
  • Staffing based upon workload
  • Clear assignment of responsibility and accountability
  • Optimized workflow and incorporation of technology
  • Able to plan ahead and implement
  • Well defined capabilities and focus
  • Each study given high priority with accessible, central contact person
  • GCP and human subjects protection training, education and certification for staff and investigators