Sponsors & CROs

Our unique model can perform your clinical trials in both private practice and community based hospital settings. Our staff is comprised of Research Director, Board-Certified Principle Investigators, Project Manager, Regulatory Analyst, Research Coordinators, Compliance and Marketing team for subject recruitment. Our investigators are GCP trained and involved in feasibility, recruitment and retention. All research coordinators are either certified or become certified once eligible.

Providing our Sponsors and Contract Research Organizations (CROs) with:

  • Unique study specific feasibility assessments
  • Site Mobilization Team for streamlined site activation
  • Clinical data integrity
  • Study enrollment metrics
  • Proven reputation with established Sponsor relationships
  • Strategic recruitment plan constructed for each Protocol
  • Nationwide research site capabilities in over 60 facilities
  • Expeditious regulatory submission
  • Established rapport with local and central IRBs
  • Proficient in Electronic Data Capture (EDC)
  • Continuous staff education
  • Proactive and responsive management teams
  • Strategic alliances with Sponsors and CROs
  • Research-friendly environments
  • Access to large databases through private practice, Principal Investigators and Sub-Investigators

Please contact us with your new study opportunities.

We are available to assist you in pre-award feasibility assessments as well as physician Protocol evaluations.