For Sponsors & CROs: Feasibility responses within 48 hours
Core Clinical Research Group delivers efficient study start-up, reliable patient recruitment, and high-quality clinical trial execution through physician-integrated outpatient sites.
Rapid Startup Support | Physician-Integrated Sites | Recruitment-Focused Operations | Compliance-Driven Execution
Core Clinical Research group partners with sponsors, CROs, and biotech organizations to support clinical trials within real-world outpatient healthcare settings.
Our model is designed to integrate research seamlessly into existing clinical workflows while maintaining strong standards for recruitment, compliance, and data quality.
EMR-assisted identification, physician referrals, and targeted outreach strategies.
Feasibility review, regulatory readiness, and activation support.
Coordinator workflows, visit scheduling, and protocal adherence.
GCP-aligned processes, source accuracy, and audit readiness.
Primary Care
Metabolic/Obesity
Cardiovascular
Infectious Disease
Preventative Medicine
Responsive feasibility turnaround
Access to real-world patient populations
Enrollment-focused operational model
Physician-integrated oversight
Scalable partnership approach
Strong communication and responsiveness
1. Feasibility Assessment
Protocol review, population fit, startup planning
2. Site Activation
Regulatory onboarding, contracts training
3. Enrollment Execution
Patient outreach, screening, retention
4. Delivery & Reporting
Clean data, sponsor responsiveness, milestone tracking
Connect with Core Clinical Research Group to discuss study opportunities, feasibility, and partnerships.
CCRG
Clinical Research Organization
Advancing clinical research through precision, speed, and compliance.
Contact
coreclinicalresearchgroup@gmail.com
727 558 9994
Canton, GA
© 2026 Core Clinical Research Group