Newsletter | July 15, 2025

07.15.25 -- What's The Risk Of Letting Researchers Use LLMs?

SPONSOR

Webinar: Unlocking Global Oncology Success: The Strategic Advantage of Australia & Asia for U.S. Biotechs

The oncology clinical trial landscape is evolving, and U.S. biotech companies are increasingly seeking innovative solutions to accelerate their drug development programs. Join us as we explore how Australia, Taiwan, and South Korea provide a strategic advantage in conducting early, mid, and late-phase oncology trials, offering speed, cost efficiency, and global scalability. Register now.

CLINICAL TRIAL TECHNOLOGY

What's The Risk Of Letting Researchers Use LLMs?

Who should be using AI and how? Sage Therapeutics' Jake Alme explores AI use in clinical research, examining its use shifting toward more complex applications and discussing the risk of using it in the public domain.

Remote Patient Monitoring Using Mobile Health Technology

This study investigates the attitudes of cancer patients towards the adoption of mHealth technologies, including applications and wearable devices, for monitoring purposes during or after their treatment.

How eConsent Delivers Value For Sponsors

Delve into the data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials.

ISPOR 2024-2025 Top 10 HEOR Trends

This report outlines ten defining HEOR trends influencing global health decision-making.

Streamline Trial Master File Documentation And Integrate With Sites

Streamline your Trial Master File (TMF) documentation and integrate with study sites to accelerate trial timelines.

Industry-First eTMF AI: PhlexTMF v21

Pre-trained on millions of documents and embedding the cumulative guidance of Phlexglobal’s TMF experts, uncover how teams can ensure clinical documents are “right-first-time” at document upload.

SPONSOR

Partnerships with Sites, held September 15, 2025, in Philadelphia, is purpose-built for clinical operations professionals looking to elevate collaboration with research sites. Through real-world case studies and strategic discussions, attendees will gain tools to reduce burden, accelerate enrollment, and build stronger sponsor-site relationships. Use code LSL20 for 20% off your registration.

SPONSOR

Discover how to apply ICH E6 R3 in practice during this expert-led discussion on risk-proportionate approaches in clinical trials. Learn how to integrate and analyze data to streamline oversight, enhance compliance, and improve patient safety. Registration for this Clinical Leader Live digital event is free thanks to the support of Revvity and Medable.

CHOOSE YOUR OWN ADVENTURE

You're receiving the Tuesday edition of the Clinical Leader newsletter, focusing on Clinical Trial Technology. To make changes to your newsletter selections, update your topic preferences.

  • 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)

Learn more about our personalized newsletters here.

Connect With Clinical Leader: