05.12.25 -- 7 Steps For Clinical Investigators To Implement A Robust AI Governance System

Get actionable strategies to enhance engagement, strengthen relationships, and support study success in clinical research through clear communication, transparency, and ethical practices.

Clinical research site coordinators are the unsung heroes of trial execution—managing complex protocols, supporting participants, and navigating fragmented systems, all while ensuring study integrity.

Learn about how this participant-friendly technology ensures efficient and secure payments, enhancing the clinical trial experience for all involved.

Eliminate financial friction points in your clinical trial financial management, ensuring trials are both operationally efficient and financially transparent.

Address the challenges of identifying the most suitable trial sites and investigators while optimizing feasibility planning, reducing screen failure rates, and improving patient retention.

When you "get your tile" into One Home, you're building up the library of systems available to sites for single sign-on and task management across their trials.

Clinical trial enrollment remains a major bottleneck in drug development, but consumer-centric innovations could present a solution to enhance every stage of clinical trial enrollment.

Despite clinical trial awareness campaigns and site expansions trials continue to fall short in reaching the patients who need them most, resulting in a shift toward community-rooted recruitment.

Explore advanced technologies that offer a remote solution to maintain rigorous standards for ECG assessment while adapting your trial to have a more patient-centered design.

Jonathan Rigby, CEO and Sernova, explains how he turned his passion for helping others into life-saving treatments for diabetes and other chronic diseases.

Clinical trials are inherently complex, and even well-structured studies may struggle to achieve statistical significance due to challenges in study design, patient selection, and data variability.

Integrating pregnant women into clinical trials through strategic partnerships, accessible trial locations, and robust informed consent processes is essential.

In 2025, it is likely the clinical trial landscape will be shaped by advancements in artificial intelligence (AI), evolving recruitment strategies, and a renewed focus on equitable access.

For biotech companies partnering with an experienced CRO ensures that patient recruitment efforts are both efficient and effective.