At JT BridgePoint Global Clinical Solutions, LLC, we help research teams deliver studies that are efficient, compliant, and patient-centered.
Our consulting spans Clinical Research Support, Regulatory and Quality Management, and Project Management & Training giving investigators, institutions, and sponsors a trusted partner to meet standards, build confidence, and achieve results.
Our Services
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Clinical Research Support
We help research teams move from planning to launch with ease — guiding study startup, IRB submissions, and patient recruitment strategies that strengthen enrollment and compliance from day one.
What you gain:
Study startup guidance
IRB submissions & protocol navigation
Tailored patient recruitment strategies
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Regulatory and Quality Management
Our expertise ensures your studies meet the highest standards. From SOP development and compliance reviews to CAPA tracking and audit readiness, we help you stay aligned with ICH-GCP and FDA expectations.
What you gain:
SOP development & compliance reviews
CAPA tracking & audit readiness
ICH-GCP / FDA standards consulting
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Project Management and Training
We keep your projects on time and on budget. JT BridgePoint coordinates vendors, streamlines sponsor communications, and provides training to build confident, inspection-ready teams.
What you gain:
Timeline & budget oversight
Vendor coordination
Sponsor communications support
Onboarding for coordinators & staff
Refresher compliance sessions
Guidance for students & junior researchers