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Commentary|Videos|April 9, 2026

How Agentic AI Will Realistically Reshape the Clinical Trial Workforce

In this video interview, Krishna Cheriath, vice president and head of clinical research digital data and AI at Thermo Fisher Scientific, introduces a practical augmentation scale for thinking about how AI agents will transform clinical trial roles over the next two years and why workforce planning for that shift needs to start now.

Full interview summary

In a recent video interview with Applied Clinical Trials, Krishna Cheriath, vice president and head of clinical research digital data and AI at Thermo Fisher Scientific, discussed how AI-driven tools are reshaping clinical operations across the full trial lifecycle—from case intake and workflow design to patient enrollment, data collection, and the emerging frontier of agentic AI. He opened by framing the current state of AI adoption around two core use cases: knowledge synthesis and applied intelligence, while making clear that the most significant barriers to successful implementation are no longer technological. The real obstacles, he argued, are the willingness to fundamentally reimagine business processes with AI by design, and the organizational commitment to upskilling the workforce to use these tools appropriately.

Cheriath emphasized that effective AI adoption requires balancing ambitious moon-shot objectives with bottom-up confidence building, and that clinical operations teams across biopharma and CROs struggle to carve out the space and time needed for meaningful innovation when day-to-day demands are relentless. He also stressed the need for boundary spanners—people who can fluently bridge clinical operations expertise and AI capability—as a critical and currently undersupplied organizational asset.

On patient centricity, Cheriath brought a notably grounded perspective, drawing on his own family's healthcare experience to argue that technology alone cannot solve enrollment and access challenges rooted in social determinants of health. He made a compelling case for using AI to reduce site administrative burden as an indirect but powerful lever for improving patient focus and care quality at the site level.

He closed with a detailed and pragmatic framework for thinking about agentic AI's impact on the clinical workforce, introducing an augmentation scale from level zero through level four and predicting that virtually all clinical trial roles will fall somewhere between levels one and three within two years—a shift he described not as a future possibility but as a workforce planning imperative for today.


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© putilov_denis - © putilov_denis - stock.adobe.com
Real-time clinical trials require standardized digital data capture at the point of care through scaled eSource-EDC-EHR integration, but progress stalls because competing standards lack regulatory enforcement and one-off system integrations cannot scale beyond single studies without industry-wide alignment and legal clarity on data ownership.
© photon_photo - © photon_photo - stock.adobe.com
Standardized measurement across five oncology centers found that clinical research coordinators rated eSource-enabled workflows positively (Overall Mean Satisfaction 5.79 of 7), with reduced manual entry and electronic data transfer earning strong marks, while perceived reduction in sponsor and monitor queries lagged as the one domain below threshold.