Why Choose Us?
Your Trusted Partner for Seamless, Inclusive Clinical Trials
At SitePath Clinical Research, we accelerate clinical trials through a centralized, physician-led site network backed by deep industry expertise and advanced research technology. Our commitment to diversity drives inclusive participation by expanding access to underserved and underrepresented communities—bringing innovation where it’s needed most.
From study startup to closeout, we provide comprehensive, full-service support focused on transparency, regulatory excellence, and collaborative execution. Our streamlined processes reduce delays and improve efficiency, enabling Sponsors and CROs to meet timelines without compromising quality or compliance.
With access to millions of consented patient records, thousands of enrolled patients, and a 91% retention rate, SitePath delivers reliable, measurable results—every time.
21 Years Of Excellence
Trusted Research Partners
At SitePath Clinical Research, we work in close partnership with leading Sponsors and Contract Research Organizations (CROs) to accelerate medical innovation. These collaborations are grounded in integrity, scientific excellence, and an unwavering focus on patient safety.
By aligning with global leaders in clinical development, we ensure that every trial is conducted to the highest standards—delivering quality data, regulatory compliance, and meaningful clinical outcomes. Together, we’re shaping the future of healthcare by advancing life-changing therapies to the patients who need them most.
Our Key Strengths
Explore how our commitment to operational efficiency, inclusive research, and uncompromising quality sets SitePath apart—consistently delivering exceptional value to our partners.
- Efficiency and Speed
- Diversity and Reach
- Quality Assurance
- Staff Experience
Efficiency and Speed
At SitePath Clinical Research, we streamline the clinical trial process from startup through closeout. Our centralized site management, advanced digital platforms, and experienced regulatory team drive faster study activation and shorter turnaround times. We eliminate delays without sacrificing quality—helping Sponsors meet critical milestones on time.
Diversity and Reach
We are deeply committed to improving access to clinical trials by engaging diverse and underserved populations. Our investigator network spans a broad spectrum of geographic, ethnic, and socioeconomic backgrounds—ensuring inclusive recruitment and meaningful, real-world outcomes. For us, diversity is more than a metric—it’s a mission.
Quality Assurance
Quality is embedded in every step of our process. From proactive protocol compliance to continuous data oversight, we uphold the highest regulatory and scientific standards. Our internal QA systems, GCP-certified staff, and secure eSource/eRegulatory tools ensure data accuracy, integrity, and full compliance throughout the trial lifecycle.
Staff Experience
Our team brings decades of combined clinical research experience across a wide range of therapeutic areas. With bilingual staff, experienced coordinators, and board-certified principal investigators, we offer knowledgeable, responsive, and compassionate support at every phase. Our people are your competitive advantage.
Our Results
Successful Mission
99%
Researches
80%
Costumer Satisfaction
90%
Sponsor's Trust
92%
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