Meet with Everest at
Medidata Next and Phuse Connect
Turning complex clinical data into confident, submission-ready decisions.
Complete the form to schedule a meeting with our team at one of our two March conferences and let's discuss how we can support your next clinical study.
Medidata NEXT
March 10–11 | New York, NY
Roundtable Discussion: 12:15 - 1 p.m.
As a Medidata Accredited Partner, Everest has completed comprehensive training across the Medidata platform.
Our experts understand not just how the technology works — but how to apply it to drive efficiency, quality, and compliance across your studies.
Our Clinical Data Management team will be in attendance to answer your questions and discuss your study's needs.
Phuse Connect
March 22–26 | Austin, TX
Everest brings deep expertise across the full biometrics spectrum, with strong capabilities in biostatistics, statistical programming, and regulatory-ready data delivery.
Meet with our biometrics experts on-site to discuss your upcoming clinical studies, as well as how we can provide high-quality, submission-ready data that you can trust.
Schedule a Meeting
Why Sponsors Repeatedly Choose Everest
Operational excellence you can feel. We deliver clinical trials with a level of rigor, responsiveness, and reliability that sponsors consistently say is rare in our industry.
Customer service that stands out. Our teams act as true extensions of yours—proactive, highly engaged, and committed to solving problems before they become barriers.
Data strength built into our DNA. As a biometrics provider turned full-service CRO, we bring a deep, data-first mindset to every study. That means cleaner data, fewer surprises, and faster decision-making.
Flexibility at its core. We can deliver support exactly how you need it: Project-based or turn-key (full-service or selected services), FSP, unit-based or time and materials.
About Everest
Our story began more than 20 years ago as a dedicated biometrics service provider. Over the last decade, we’ve evolved into a full-service CRO—bringing the same data-driven discipline, scientific rigor, and precision to every part of clinical trial delivery.
Today, we’re a global organization with offices across North America, Europe, and Asia, and a team of more than 700 experts. We’re small enough to stay nimble, responsive, and personalized—yet large enough to deliver the global experience and operational strength required for successful clinical trials.