Clinical Trial Programs

Clinical research should gather more than just data. It should find truths. And the knowledge that’s uncovered through this process should be shared so that it can be put into practice more quickly—helping real people in real-world settings. That’s what the approach to clinical studies should be, and that’s what we do at the DCRI.

Comprehensive Capabilities for Confidence at Every Phase

Applying thought leadership from physician-researchers and leading biostatisticians to study protocols is essential. But having the expertise, technology, and resources to successfully conduct studies can lead to results that impact care sooner. This is what sponsors count on and receive when they work with the DCRI. From design to implementation to publication, the DCRI manages every facets of clinical research. This gives our sponsors the confidence their studies are being managed seamlessly throughout all clinical research phases by practicing physicians and data and operational experts who know exactly what’s at stake.

group photo

Worldwide Operational Excellence

Experienced and consistent Clinical Operations teams expertly manage all aspects of global clinical trials. Additionally, impeccable data integrity and biostatistical expertise yield credible study results that change clinical practice.

Our operational capabilities include:

  • Full-service expertise across all phases of development (phases I–IV)
  • Pharmacometrics
  • S. Rapid Start Network (RSN)
  • Therapeutically focused project leadership and site management
  • Global regulatory support
  • Pharmacogenomics
  • Health outcomes research
  • Adaptive trial designs
  • Event adjudication
  • Safety
  • Viral monitoring