The infrastructure behind smarter clinical trials

Full-service clinical trial execution and regulatory support

The infrastructure behind smarter clinical trials

Full-service clinical trial execution and regulatory support

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The right strategy today shapes the approvals of tomorrow

The infrastructure behind smarter clinical trials

Executing a successful clinical trial requires more than just a great strategy—it demands seamless execution, quality oversight, and proactive risk management. At Rho, our capabilities extend across the entire clinical development lifecycle, ensuring that every trial is conducted with precision, efficiency, and patient safety in mind. From expert project management to pharmacovigilance, we provide the foundation that makes breakthrough research possible.

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Why Rho?

Why Rho?

Integrated clinical operations
A full-service approach to trial management, from startup to closeout.
Proactive risk-based quality management
Identifying and mitigating challenges before they become obstacles.
Dedicated site and investigator relationships
Strong partnerships that improve study efficiency and data integrity.
Patient safety and pharmacovigilance expertise
Ensuring the highest standards of regulatory compliance and oversight.

Ready to execute your trial with confidence?
From project management to patient safety, Rho provides the capabilities that drive clinical success. Let’s make it happen.

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Matt Healy

Mr. Healy can turn the most complex CNS-centered trials into something that runs smoothly. With deep expertise across clinical operations, project management and delivery, and pharmacovigilance, he’s led and supported Phase 2-4 studies from kickoff to conclusion, both domestic and worldwide. His work has spanned indications, including Alzheimer’s Disease, Late-Life Depression, and Traumatic Brain Injury, among others. Both strategic and grounded, Mr. Healy is known for keeping project teams focused, timelines tight, and making even the toughest studies look easy. Mr. Healy is the steady force that can keep studies moving while maintaining quality and consistency for sponsors.

Heather Kopetskie

After more than two decades at Rho, Ms. Kopetskie knows that behind every strong clinical trial is an even stronger dataset to support the study’s findings. Her background spans everything from protocol development, analysis of clinical data, writing and reviewing statistical reports, and more. Her therapeutic experiences include CNS, infectious disease, transplantation, and additional indications. As the VP of Global Biometrics, Ms. Kopetskie manages a high-performing team of statisticians and programmers—she doesn’t just lead the numbers, but also the people behind them. With her sharp eye and calming force, she can help project teams turn complex data into knowledge.