- 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
