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SCOPE 365 is the year-round digital extension of SCOPE, bringing clinical research professionals continuous access to insights, live virtual meetups, expert interviews, and premium intelligence products. It’s a centralized hub designed to help sponsors, CROs, sites, and solution providers stay on the pulse of the industry, elevate thought leadership, and maintain momentum between SCOPE’s global conferences.

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Insights from SCOPE

  • Rethinking Rare Disease Recruitment in the Era of Genomic Data

    Insights from SCOPE | Challenges around rare disease recruitment aren't always about patient volume. Precision matters. When eligibility depends on specific mutations or biomarkers, traditional funnels fall short. Learn how mutation-aware outreach and structured data can connect the right patients to the right trials faster.

    May 7, 2026

  • Bringing Real-World Data Upstream in Patient Recruitment Planning

    Insights from SCOPE | Most recruitment challenges don’t begin when enrollment stalls. They start months earlier in protocol design and feasibility assumptions. Learn how bringing real-world data upstream can prevent downstream delays, reduce screen failures, and improve enrollment predictability before the first patient is contacted.

    May 5, 2026

  • What Real-Time FDA Oversight Means for Clinical Operations

    Insights from SCOPE | The FDA’s move to pilot real-time clinical trial data access is a signal of where the industry is heading, not a sudden change in direction. For years, clinical operations teams have been working toward faster, more connected ways of generating and acting on data. What’s changing now is who participates in that environment. Instead of reviewing submissions after the fact, regulators are beginning to explore what it looks like to engage with trial data as it evolves. That shift, from periodic review to continuous visibility, creates an opportunity to rethink how trials are designed, executed, and monitored. For clinical teams, this is less about disruption and more about alignment with work already in progress.

    Apr 30, 2026

  • AI in Study Startup: Speed With Guardrails

    Insights from SCOPE | CRFs, edit checks, statistical analysis plans, protocol abstractions. Study startup artifacts are highly structured, deeply interdependent, and almost always time-compressed. They are also repeatable. Within a therapeutic area, much of the logic behind these artifacts is reused across studies. Visit schedules follow familiar patterns. Edit-check rules draw from established standards. Statistical plan sections mirror protocol language with predictable mappings. Despite this, teams frequently rebuild them manually, adapting prior versions line by line under tight timelines. That manual rebuild cycle adds weeks to startup and introduces inconsistency that surfaces later during data cleaning or regulatory review. AI is beginning to change this phase of development, but the real opportunity is not just faster drafting. It is controlled acceleration.

    Apr 28, 2026

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What You’ll Find in SCOPE 365

SCOPE of Things Podcast

SCOPE of Things

The Scope of Things podcast explores clinical research and its possibilities, promise, and pitfalls. Clinical Research News Senior Writer, Deborah Borfitz, welcomes guests in the field.
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Voices of SCOPE

Voices of SCOPE

Voices of SCOPE brings you unfiltered conversations with the people driving change in clinical research. These straight-talk interviews spotlight real lessons, fresh ideas, and practical innovations from leaders across pharma, biotech, tech, and patient advocacy.
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SCOPE Summaries

SCOPE Summaries

Concise, accurate summaries of key presentations from SCOPE Summit U.S., SCOPE Europe, and SCOPE X, designed to help you quickly absorb what matters most.
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SCOPE Summit
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SCOPE X
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