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Are research sites doing everything twice for no good reason?
In this Sticky Notes episode, Denali and Brad get real about eSource, EDC, and who should actually own site-facing tech. They move past the buzzwords and tackle the uncomfortable questions:
Why is sponsor tech so fragmented for sites? If we're already entering everything into EDC, why do we still need separate source? Why isn't direct data capture the default? What do regulations and audit trails really require from sites? Are sponsors truly becoming "site-centric", or just saying that on stage at conferences? They also hit on duplicate data entry, interoperability, private equity–backed sites, and how real-life clinic workflows clash with sponsor systems.
If you run or work at a research site—and you're tired of logging into 10 portals per study—this conversation is for you.
🔔 Subscribe for more blunt, practical discussions on clinical trial operations, site life, and research tech that actually works (or doesn't).
By Brad Hightower4.9
2727 ratings
Are research sites doing everything twice for no good reason?
In this Sticky Notes episode, Denali and Brad get real about eSource, EDC, and who should actually own site-facing tech. They move past the buzzwords and tackle the uncomfortable questions:
Why is sponsor tech so fragmented for sites? If we're already entering everything into EDC, why do we still need separate source? Why isn't direct data capture the default? What do regulations and audit trails really require from sites? Are sponsors truly becoming "site-centric", or just saying that on stage at conferences? They also hit on duplicate data entry, interoperability, private equity–backed sites, and how real-life clinic workflows clash with sponsor systems.
If you run or work at a research site—and you're tired of logging into 10 portals per study—this conversation is for you.
🔔 Subscribe for more blunt, practical discussions on clinical trial operations, site life, and research tech that actually works (or doesn't).

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