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Research Services


  • Rapid, In-depth protocol feasibility reviews
  • 48 hour turn-around of regulatory documents and IRB submissions
  • Dedicated, fulltime Research Nurses (CCRs)
  • Accelerated budget and contract reviews
  • Expedited site start-up and source document development
  • Dedicated regulatory, data entry, and recruitment staff
  • EMR-driven screening and enrollment of study subjects
  • Strict protocol adherence
  • Consistently accurate and clean data