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Riley Farley

Bring Your Own Technology (BYOT) Playbook Offers Roadmap for Using Site-Based Tools in Pharma-Sponsored Trials

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RealTime eClinical Solutions co-authors industry-first guide for sponsor-site collaboration on technology choice.  San Antonio, TX – October 7, 2025 – When clinical research sites use the technology they know best, trials move faster, data is cleaner, and compliance risk drops. That’s the vision behind the new Bring Your Own Technology (BYOT) Playbook, a practical, field-tested guide developed … Read more

A Site Selection Framework That Actually Works: Introducing TrialAlign

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Site selection in clinical trials is stunted, often driven by past relationships and familiarity. In fact, studies show that in any given multi-site trial, about 70% of participating sites were previously used by the sponsor1. While there are advantages to reusing known sites, like faster contracting, established workflows, and existing relationships, past collaboration doesn’t always … Read more

The Hidden Cost of “Free” eClinical Systems: Why CTMS and eReg Are Too Critical to Cut Corners

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In clinical research, budgets are always under pressure. So, when a sponsor, CRO, or vendor offers a “free” system, whether it’s a Clinical Trial Management System (CTMS) or an eRegulatory (eReg) platform (also called an electronic Investigator Site File, or eISF), it can sound like a welcome relief.  But as many Academic Medical Centers (AMCs), … Read more

RealTime eClinical Solutions Wins Dual Honors for Innovation and Marketing in the 2025 Clinical Trials Arena Excellence Awards

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About RealTime eClinical Solutions San Antonio, TX – September 18, 2025 – We are proud to announce that RealTime eClinical Solutions has won the Innovation and Marketing awards in the 2025 Clinical Trials Arena Excellence Awards. The recognition underscores our commitment to advancing technology and elevating our brand to better serve the clinical trials industry.  The Clinical … Read more

CTMS vs SOMS: Why Your Site Needs a Unified eClinical Toolkit

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Clinical trials are moving faster, growing more complex, and facing sharper regulatory scrutiny than ever before. That leaves clinical research sites and site networks with a critical question: is your technology helping you move faster? For too many sites, the answer lies somewhere in the middle.  That’s why we’re exploring a unified approach to clinical trial … Read more

RealTime eClinical Solutions Launches TrialAlign: Transforming Clinical Research Site Selection and Feasibility with Unbiased Performance Data 

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Complete profile published here: RealTime eClinical Solutions is an enterprise-grade technology provider and a Dual Category Award Winner in the 2025 Clinical Trials Arena Excellence Awards San Antonio, TX – September 3, 2025 – RealTime eClinical Solutions announces the launch of TrialAlign, a groundbreaking site selection, feasibility, and performance analytics platform designed to help sponsors … Read more

Ask the Expert: How Can Clinical Research Sites Turn Interest into Enrollment?

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Ask the Expert - How clinical research sites can turn interest into enrollment

Featuring Rick Greenfield, Founder and Chief Strategy Officer at RealTime eClinical Solutions.  Locating patients interested in a clinical trial is hard. But getting them enrolled? That’s often where the real challenge begins.  In this edition of Ask the Expert, we speak with Rick Greenfield, Founder and Chief Strategy Officer at RealTime eClinical Solutions and former … Read more

Webinar Recap: Site Selection Strategies in 2025 -Leveraging Data-Driven Metrics for Success

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Based on insights from the Xtalks hosted webinar: Site Selection Strategies in 2025.  Clinical trial site selection has never been more competitive, or more critical. Protocols are more complex. Timelines are tighter. And sponsors can no longer afford the delays, deviations, or dropout rates that come from choosing the wrong sites.  That was the focus … Read more

What Every CRC Should Know About CTMS: Tips, Tools, and Time-Savers

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Clinical Research Coordinators (CRCs) are the unsung heroes of clinical trials. They manage visits, communicate with participants, complete source data, handle sponsor queries, and keep everything moving, often across multiple studies at once. But with growing protocol complexity, tighter timelines, and more tech than ever, the job isn’t getting easier. That’s why a Clinical Trial … Read more

Reducing Redundant Regulatory Work: The Compliance Officer’s Guide

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reducing redundant regulatory work in clinical trials

About the Author: Michele Corvino, Vice President of Product at RealTime eClinical Solutions, has more than 25 years of product management experience at companies such as Oracle, IBM Smarter Workforce, and Complion. As VP of Product, she designs and creates innovative solutions that improve clinical research efficiencies and helps customers focus on research and maximizing … Read more