About Complete Clinical Research
Founded by Dominique Fuller, CCRA, a clinical research professional with more than 10 years of experience supporting sponsors, CROs, investigators, and research sites, Complete Clinical Research provides practical GCP compliance, quality, and operational support designed to strengthen research operations and maintain inspection readiness. With experience spanning study startup, site management, monitoring, regulatory compliance, and quality oversight, CCR helps organizations strengthen research operations while maintaining inspection readiness and adherence to industry standards.
Key Highlights
• Certified Clinical Research Associate (CCRA) since 2018
• 10+ Years of Clinical Research Experience
• Experience Supporting Sponsors, CROs, Investigators, and Clinical Research Sites
• Expertise in GCP Compliance, Quality Systems, and Regulatory Operations
• SOP Development, Staff Training, and Site Readiness Support
Meet The Founder
Meet the Founder
Dominique Fuller, CCRA, is a clinical research professional with more than 10 years of experience supporting sponsors, CROs, investigators, and research sites.
Throughout his career, he has contributed to study startup, site activation, monitoring, regulatory compliance, quality oversight, and operational improvement initiatives.
Through Complete Clinical Research, Dominique provides practical compliance, SOP development, site readiness, and training solutions designed to strengthen quality systems and improve inspection readiness.
Our expertise
GCP Audits
sop development
training program
site start-up Assistance
Comprehensive evaluations of site practices to ensure compliance with regulatory standards.
Creation and customization of standard operating procedures tailored to your site.
GCP-focused staff training to enhance operational efficiency and compliance awareness.​
Guidance and support in launching new clinical research sites.
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Operating Hours
Monday-Friday: 9am to 5pm
