We are a Miami-based clinical research site specializing in urology and oncology studies, delivering reliable execution across Phase I–IV clinical trials.
Our strategic location in South Florida provides access to a highly diverse patient population, allowing us to support studies that require specific demographics and complex eligibility criteria. This diversity strengthens enrollment performance and supports broader clinical applicability.
We maintain direct access to patients through an established internal database, as well as active collaboration with private practices, specialists, and referral networks. This enables us to consistently identify and pre-screen qualified participants without relying solely on external recruitment strategies.
Our site is equipped with in-house capabilities including biopsy procedures, cystoscopy, and local laboratory support, ensuring efficient protocol execution and reduced operational delays. With dedicated exam rooms and optimized patient flow, we are structured to support both standard and complex study designs.
For every study, we implement structured workflows focused on enrollment efficiency, patient retention, and protocol compliance. Our team maintains proactive communication with participants, contributing to strong retention rates and high-quality data delivery.
A specialized clinical research site built for speed, precision, and reliable enrollment in urology and oncology trials.
01
Proven Enrollment Capabilitytap >
We don’t rely on passive recruitment.
Our established patient database and active physician network allow us to identify and pre-screen qualified participants quickly—reducing startup delays and accelerating enrollment.
02
Specialized Clinical Focustap >
We focus on urology and oncology, enabling deeper protocol understanding, better patient matching, and more efficient study execution across Phase I–IV trials.
03
Reliable Execution & Data Qualitytap >
Our experienced team ensures strict protocol adherence, high patient retention, and clean, audit-ready data—minimizing risk for sponsors and CROs.
Consistent Patient Enrollment
We leverage a well-established patient database and active referral network to ensure a steady flow of pre-qualified participants—reducing recruitment timelines and minimizing screen failures.
High-Quality Execution & Compliance
Our team operates under strict clinical and regulatory standards across Phase I–IV trials, ensuring protocol adherence, accurate data collection, and audit-ready performance at every stage.
Strong Patient Retention
Through proactive communication and patient-centered coordination, we maintain high retention rates—supporting study completion and data integrity.
Victor M. Soto
Clinical Trials Project Director & Lead Coordinator
Ericka Sutherland
Clinical Research Coordinator


