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Clinical Trial Events
SCOPE Europe 2026

Talk Trial Design and Protocol Development track

The Protocol That Almost Wrote Itself—How AI Transforms Study Design, Protocol Digitisation, and Clinical Document Authoring

Wed, Oct 14, 2026 · 1:55–2:20 PM CEST InterContinental Barcelona

About this session

Sponsored by Evinova. The protocol is the single most consequential document in any clinical programme, yet it's too often treated as a static PDF rather than a structured digital asset. This interactive session brings together pharma leaders and technical experts to explore three concrete ways AI is reshaping the protocol lifecycle: Mining the past—Turning decades of trial history into a queryable knowledge Designing before committing—Using simulation and real-world data to stress-test eligibility criteria and enrolment assumptions Authoring beyond the protocol—Generating and maintaining consistency across downstream documents (ICF, SAP, eCRF) as the protocol evolves Rather than a technology showcase, this is a working conversation: panelists share where AI is already delivering value, and attendees are invited to weigh in on where their own organisations stand—and what's really holding transformation back.

Speakers

  • Pablo Chirosa Lara

    Senior Commercial Director, AI Enabled Clinical Development · Evinova

    Speaker

  • Francesco Multari

    Director, Data Science · Evinova

    Speaker

  • Gernot Weber

    Senior Director, Head of Data Strategy & Products, Global Functions · Johnson & Johnson Innovative Medicine

    Speaker

  • Maria Bowen

    Head of Protocol Excellence, Clinical Science · Daiichi Sankyo

    Speaker

  • Carlos Erasun

    Medical Director, Early Global Dev, Oncology R&D · AstraZeneca

    Speaker

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