News & Insights
A Day in the Life of a Site Coordinator (That Nobody Sees)
If you want to understand clinical research, spend one day in the life of a site coordinator. Not the polished version seen on dashboards or in monitoring reports — but the real day. The day woven together by competing priorities, human emotion, protocol demands, and a constant stream
Where Rigor Meets Reality: Designing Protocols for Real-Life Patients
Too often, protocols are written for a version of patients and clinics that doesn’t exist—one with unlimited flexibility, perfect adherence, and no competing life demands. When design ignores reality, it quietly limits access, reduces diversity, and creates operational barriers that sites must absorb, even though smarter, more flexible design can
Clinic Integration Guide
Expanding Your Medical Practice into Clinical Research This expanded guide offers clinics a roadmap to planning the steps needed for successfully integrating clinical research into existing medical practice. With practical steps and key insights, Ridge Research Solutions equips clinics to grow research services while protecting patient care. The
How Sites Should Price DCT Work in Budgets and Contracts
When decentralized or hybrid study models are introduced, the industry often talks about patient convenience, expanded reach, and flexibility. BUT – what does it actually cost a site to run a decentralized trial? And how should sites price that work in a way that reflects reality, scale, and sustainability? Sponsors often treat
The Budget Blueprint
How Sites Can Build Rate Cards, Avoid Revenue Gaps, and Negotiate with Confidence This guide is designed to help clinical research sites understand the importance of building strong budgets and developing rate cards. By mastering financial preparation, sites can protect themselves from revenue gaps, sustain operations, and build credibility with
How Many 1572s Is Too Many?
Cutting Through the Confusion Around Repeated Form FDA 1572 Updates Do you find yourself asking this question every time you’re asked to resubmit a Form FDA 1572? Is it being clearly explained as to why it was requested – and what happens if you push back on the request? It’s