| | | | Webinar: Avoid the Wrecking Ball: Targeted Solutions for Struggling Trials | When a trial starts slipping off track, the instinct is often to “rescue” it — swap vendors, replace sites, or overhaul teams. But these costly moves usually treat symptoms, not the cause. The real problems often run deeper: misaligned protocols, overburdened sites, and unclear operational ownership. Discover how to fix what’s broken without hitting reset, so you stay on track, protect budgets, and deliver for patients. |
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| | | Closing The Gender Gap In Clinical Trials With Digital Devices | Guest Column | By Anita Phung, MRGCP, MRCP, MBBS, BSc (Hons), research physician | For decades, women have been underrepresented in clinical trials — a gap that’s not just unfortunate but dangerous. Digital devices might be the difference maker, says research physician Anita Phung, MRGCP, MRCP, MBBS, BSc (Hons). |
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| | Move The Needle On Clinical Research | Brochure | EmVenio Clinical Research | Adaptable to any trial study, this team of experienced Certified Mobile Research Nurses travels directly to your trial participants, wherever they may be — at home, work, school, care centers, and more. |
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| Join industry leaders at the IRT conference in Boston, October 14-15, 2025, at The Westin Copley Place. This key event brings together the clinical supply community to explore cutting-edge technology updates, optimized data collection strategies, and innovative solutions for randomization and trial supply management. Network with experts and discover operational strategies to streamline clinical research and trial data management. Use VIP code IRT25LSC for 10% off when registering. |
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| | | Why More Biotechs Are Starting Trials In Australia | From The Editor | By Dan Schell, chief editor, Clinical Leader | Why are so many U.S. biotechs heading to Australia for their first-in-human trials? Speed, cost, and simplicity. In our latest piece, Megan Robertson and Tina Soulis break down how sponsors can move from protocol to first patient in just a few months—while saving money and generating data regulators will accept worldwide. |
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| | | Designing More Representative Trials Through Strategic Planning | White Paper | By Rachael Fones, Robert Stolper, Shahrzad Salmasi, Ph.D., Leslie Henderson-Williams, Monica Goins, and Eric Martinusen, IQVIA Safety & Regulatory Compliance | Strategic planning for representative clinical trials improves outcomes, regulatory alignment, recruitment efficiency, and commercial value by ensuring study populations mirror real-world patients. |
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| | | | | Central IRB Services | Product | BRANY | With BRANY Central IRB Services you’ll get: competitive pricing, collaborative teamwork, solution flexibility, expert committee and IRB staff. |
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| You're receiving the Wednesday edition of the Clinical Leader newsletter, focusing on Decentralized Trials and Trial Management. 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)
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