Regulatory Document Support
Ensure GCP
compliant, IRB-ready documentation
from the start.
Study Start-Up Guidance
Streamline activation with our expert-led startup frameworks.
Feasibility &
Site Readiness Coordination
Match the right sites
with your study—and
prepare them to
launch.
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Patient Recruitment Strategy Design
Project Management Oversight
Optimize diverse enrollment with AI-powered targeting.
Lean, experienced coordination for smooth trial execution.
At VertexCTM, we help sponsors and CROs accelerate study timelines, reduce operational costs, and increase site engagement through a streamlined, expert-driven approach. By focusing on efficient feasibility, proactive communication, and tailored support strategies, we ensure sites are better prepared, more responsive, and fully invested in study success — driving faster activations and stronger long-term partnerships.
VertexCTM offers scalable, precision-based trial support that seamlessly integrates into your study operations. Whether you need targeted site outreach, regulatory coordination, or full-service startup management, our flexible solutions adapt to your needs — delivering high-quality, audit-ready results without the overhead of traditional models. Plug in our expertise exactly where you need it to keep your trials moving forward with speed and precision.
Ensure your studies start strong with expert support in feasibility, site readiness, and regulatory compliance. At VertexCTM, we help you identify the right sites, prepare teams for activation, and navigate complex regulatory requirements with confidence. Our hands-on approach minimizes delays, strengthens site performance, and sets your trial up for long-term success.
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Expertise in Rare
&
Neurodivergent Population
Ready to bring clarity and
control to your clinical trials?
Download Our Capabilities Deck
Fill out this short form to get all the information you need from our Capabilities Deck
