At Synapse Trial Services, we are dedicated to elevating the standard of clinical trial site management through precision, partnership, and operational excellence. As a specialized Site Management Organization, we focus on empowering sponsors and CROs by delivering reliable, high-performing research sites and streamlined study execution.
Our team brings together seasoned clinical research professionals, site leaders, and operational specialists who understand the complexities of trial delivery. We support studies from feasibility and site selection through patient recruitment, enrollment, monitoring support, and close-out—ensuring each site is equipped to perform at the highest level.
Our core capabilities include site operations, patient engagement and retention, regulatory and ethics coordination, on-site trial management, and continuous quality oversight. Additionally, we provide expert staffing and resourcing solutions to help sponsors and partners access knowledgeable site personnel and study coordinators.
At SynapseTrials Services, we are committed to reducing site burden, accelerating timelines, and strengthening the foundation of every clinical trial. We work as your trusted partner to deliver efficient, compliant, and patient-centric research that moves your programs forward with confidence.”
To deliver exceptional, patient-centered clinical site management by upholding the highest standards of quality, ethics, and FDA regulatory compliance. We are committed to supporting investigators, empowering participants, and enabling sponsors to accelerate safe, efficient, and impactful medical breakthroughs.
To become a trusted leader in site management, recognized for transforming the clinical trial experience through innovation, operational excellence, and unwavering dedication to patient safety. We strive to advance global health by helping bring life-changing therapies to the patients and communities who need them most.
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