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Riley Farley

Why Building an Enterprise Operating Model for Clinical Trials Starts With eSource

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The operating model for clinical research is shifting. Protocols are becoming more complex — more endpoints, more procedures, more oversight. In tandem, clinical research site networks and multi-site organizations are scaling rapidly, expanding across more studies, more sites, and more complex portfolios. But execution hasn’t kept pace.  While trial complexity has accelerated, operational visibility has not.  For sponsors and CROs, … Read more

RealTime Webinar Recap – The eClinical Command Center: Rethinking the Research Operating Model for AMCs and Hospitals

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Watch the Replay: The eClinical Command Center: Rethinking the Research Operating Model for AMCs and Hospitals    Most Academic Medical Centers (AMCs) and hospital-based research organizations don’t lack technology. They’re operating in environments where that technology was never designed to work together.  Over time, research operations have been built around tools that are familiar, accessible, and often free. Individually, these tools work. But … Read more

How eSource Turns Clinical Trial Capacity into Revenue Growth

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Clinical research sites rarely struggle with opportunity. What they struggle with is capacity.  Clinical research coordinators (CRCs) are buried in regulatory binders, monitors occupy office space for days at a time, and the sheer volume of manual transcription creates a hard ceiling on growth. A site may have the investigators, the patient population, and even … Read more

Outgrowing Your CTMS? Why Site Networks Are Switching for Better Financial Visibility

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As clinical research site networks grow, one issue consistently rises to the top: the financial reporting inside their Clinical Trial Management System (CTMS) isn’t built for scale.  Many organizations begin with a basic CTMS, but as sites expand across locations, sponsors, and complex protocols, financial complexity increases, and system limitations become glaringly visible. This is why more multi-site … Read more

Why Multi-Site Research Organizations Struggle to Maintain a True System of Record

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In multi-site clinical research, data rarely lives in one place. What organizations call a “system of record” is often a patchwork of tools that capture only fragments of operational truth. Leaders may believe they have a system of record because they use a CTMS, shared drives, dashboards, or project boards. In reality, most organizations operate with multiple partial systems … Read more

Why Integration Alone Fails in Enterprise Clinical Research

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Why integration alone fails in enterprise clinical trials, and what AMCs, hospitals, and health systems need instead    Academic Medical Centers and large health systems have invested heavily in research technology, especially over the past decade. Most operate with electronic data capture systems, regulatory document repositories, Clinical Trial Management Systems (CMTS), financial platforms, and internal collaboration tools.   From … Read more

What an eClinical Command Center (SOMS) Actually Changes in Clinical Trials 

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Why academic and health system research organizations are rethinking “free” platforms  Most Academic Medical Centers, health systems, and hospitals don’t lack technology. They lack a unified operating layer governing research execution.   Over time, research operations are stitched together from tools that are familiar, accessible, and often free:  Systems like REDCap for data capture  SharePoint for document management   Email for coordination  Spreadsheets for … Read more

What’s Broken in Clinical Trial Oversight

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Why Site Network Leaders Need a New Layer of Operational Intelligence to Scale, Compete, and Win   Site networks have become the dominant operational model in clinical research. Sponsors and CROs increasingly rely on networks to deliver consistent performance across multiple geographies, investigators, and patient populations.   This shift has elevated the role of site network leadership. The … Read more

How AI Is Changing ClinicalTrials.gov and Why Trial Execution Still Matters 

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AI Can Read the Trial Registry. Institutions Still Have to Run the Trials.  For decades, clinical research teams have relied on the same public source of truth to understand the global trial landscape: ClinicalTrials.gov.  It’s where sponsors register studies, where regulators ensure transparency, and where research institutions look to understand what trials exist, who is running them, and how … Read more