Newsletter | April 11, 2024

04.11.24 -- Dear Data Analysts, AI Is Not Replacing You

SPONSOR

Webinar: An Introduction to One Home for Sites - Help build the only industry-wide solution to clinical trial tech overload

Increasing technology demands on clinical research sites have led to technology overload resulting in sites struggling with less capacity to run trials. Join us in this webinar to explore how to alleviate the burden on sites and still gain the benefits being delivered by clinical technology innovators. Click here to learn more.

FEATURED EDITORIAL

Dear Data Analysts, AI Is Not Replacing You

By Dan Schell, chief editor, Clinical Leader

Deep beneath the ongoing narrative of AI’s potential use cases in clinical trials is the same fear that persists in other industries facing this technology revolution. Namely, will jobs be lost and replaced by machines? So, I thought I’d ask an expert — a machine.

INDUSTRY INSIGHTS

Achieving Faster, Simpler Validation Through Crowdsource UAT

Article | By Lou Pasquale, IQVIA Technologies

An approach most often seen in the larger tech space, crowdsource UAT can offer several potential advantages for the clinical trial industry and eTMF validation.

Bringing Flexibility And Efficiency To Your Clinical Trials

Webinar | Castor

Discover why and how flexible ePRO technology revolutionizes the clinical trial experience, making it more patient-centric and more efficient for sponsors.

Data Hippies, Real-World Evidence, And Precision Medicine

Podcast | Oracle Life Sciences

Christopher P. Boone, Ph.D. discusses how democratized data and clinical innovation are moving us closer to the widespread adoption of precision medicine.

One Day, Clinical Trials Will Represent The Real World

Article | Komodo Health

What needs to happen for RWE to reach its full regulatory potential? We discussed this with industry leaders during the One Day Summit, and here are some key takeaways.

Why Now Is The Right Time To Adopt eConsent

Article | By Kate Yawman, Advarra

As much as eConsent helps staff, participants are also likely to prefer it over traditional paper methods. Explore the benefits of eConsent and some strategic steps sites can take right now to adopt the process.

How Electronic Source Data Revolutionizes Clinical Research

Article | Castor

By increasing interoperability and embracing digital solutions, see how the research community can maximize the benefits offered by eSource, leading to improved trial outcomes and data quality.

Moving Beyond Traditional CTMS To Unlock Value In An Outsourced Model

White Paper | eClinical Solutions

The proliferation of data sources and the rise of outsourced trials has changed how CTMS is defined. What role does a CTMS play in the modern-day clinical trial and are you future-ready?

Information Security Is Vital For Decentralized Trials

Article | By Phillip Winters, MRN - Medical Research Network

In today's tech-driven world, information is vital to businesses and data protection is essential. Uncover how and why teams should treat it carefully to prevent theft, forgery, or devaluation.