Services

  • Phase I – IV study capabilities
  • Inpatient and Outpatient capabilities
  • Protocol consulting – individual Investigators or as a group
  • Multiple fulltime dedicated, experienced psychometrics raters; MD, PhD and MA-level
  • Multiple full-time dedicated, experienced coordinators; CCRCs, RNs and master’s level professionals, as well as affiliated consulting specialists and pharmacists
  • Fulltime dedicated, experienced recruitment specialists and outreach coordinators
  • Access to patients – large databases, affiliated practices, large metropolitan markets
  • Well-networked for patient recruitment with chronic conditions
  • Sponsor relations team is a single source for site selection coordination to conduct one protocol across geographically diverse sites
  • Sponsor relations team provides quick turnaround on feasibilities and contracts
  • Central IRB
  • Timely/efficient start –up
  • Availability of PI
  • Consistent placebo separation data
  • Mid-study or post-study feedback – individual Investigators or as a group
  • Prior successful trial enrollment metrics
  • Sponsor and CRO relationships