Site-Based Studies

Accelerate Your Drug Development with Site‑Based Study Services

From non‑interventional prospective cohort studies and registries to chart abstractions and pragmatic trials, our site‑based services deliver the real‑world insights you need—spanning burden of illness, treatment patterns, safety evaluations, drug utilization, and patient‑reported outcomes.

Streamlined Recruitment & Network Access

With extensive access to site and clinic networks, pharmacy databases, web panels, advocacy groups, and social media, we ensure efficient identification and recruitment of representative patient populations for your site‑based studies.

How We Can Help You

Our experts can support all aspects of primary data collection for your site-based studies, including:

  • Serving as the scientific coordinating center
    • Developing protocols
    • Writing analysis plans and performing analyses
    • Writing reports and manuscripts
  • Leading and coordinating
    • Scientific advisory panels
    • Endpoint adjudication committees
    • Steering committees
  • Obtaining study approval from Institutional Review Boards and Ethics Committees
  • Managing study operations
    • Site recruitment
    • Monitoring
    • Incentive management
    • Data collection (experienced with A-CASI, EDC systems, IVRS, phone interviews, web-based, paper/fax forms, interviews, chart abstractions, etc.)
    • Data management
  • Regulatory support including preparing reports and responses to regulatory questions for studies that are conditions of drug approval 

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