Newsletter | January 30, 2026

01.30.26 -- How Can Sites And Sponsors Continuously Monitor Clinical AI

SPONSOR

Clinical research sites aren’t just execution engines. They’re the quiet architects of tomorrow’s medicines, building trust one patient at a time, solving problems no protocol can predict, and keeping trials alive when everything else wants to slow them down. Save Our Sites exists for one purpose: to build sites to last. If you’re ready to stop patching and start building something enduring… This is the conference for you. One industry. One community. Shared solutions.

TRIAL MONITORING

GCP Oversight Simplified: A Quick Guide

Discover practical, real-world strategies for sponsors to operationalize GCP oversight in a way that is collaborative, measurable, and scalable.

Expert Guidance Throughout All Your Clinical Operations

Our team of experts will guide you through the clinical trial process using a proactive and collaborative approach, ensuring that your stakeholders are always informed and confident.

CLINICAL DATA MANAGEMENT & ANALYTICS

Making AI Safety Routine: How Sites And Sponsors Can Continuously Monitor Clinical AI

Learn why the next frontier in AI governance will involve real-time surveillance of algorithmic performance across institutions with guidance from Akshaya Bhagavathula and Michelle A. Williams.

The Impact Of Expert PK/PD Modeling In Psychedelic Research

Model-informed development that integrates preclinical and literature-based data is enabling smarter predictions of exposure and safety, transforming psychedelic research and advancing clinical innovation.

AI Maturity In Clinical Development

The future of clinical research relies on operationalizing AI in a scalable, sustainable manner, ensuring that both technological and human factors are harmonized in this transformative journey.

Clinical Trials Are The Global Biopharma Industry's Biggest Headache

Explore how technology-driven, patient-centered innovation is transforming clinical trials to reduce risk, improve efficiency, and deliver smarter development outcomes.

Endpoint Clinical RTSM: Getting The Job Done

Explore how a Job-to-be-Done (JTBD)-focused RTSM approach reduces delays, optimizes costs, and accelerates trial success through predictive intelligence and streamlined global workflows.

AI In Regulatory Medical Writing: Pair Innovation With Human Expertise

AI is reshaping regulatory medical writing by accelerating document development while maintaining compliance and scientific rigor, creating regulator-ready submissions without compromising quality.

Revolutionizing Data Access With A Custom Listing Generator

Clinical teams can now access trial insights in real time using natural language to streamline workflows and accelerate decisions. Discover how to bridge data gaps with AI-powered tools.

Real-World Data And Real-World Evidence

As clinical research evolves, RWD and RWE play a crucial role in complementing conventional randomized controlled trials (RCTs) by capturing insights that accurately reflect clinical practice.

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  • Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
  • Clinical Trial Technology (Tuesday)
  • Decentralized Trials | Trial Management (Wednesday)
  • Outsourcing Models | Regulatory & Compliance (Thursday)
  • Clinical Data Management & Analytics | Trial Monitoring (Friday)

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