Ideal Clinical Research has been conducting high-enrollment vaccine trials in underserved communities since 2013. Our experienced team ensures efficient recruitment, high-quality data collection, and full regulatory compliance.
Our board-certified Principal Investigators (PIs) and Sub-Investigators have extensive clinical trial and vaccine research experience across multiple therapeutic areas.
• Diverse Recruitment Channels: We access multiple databases, including private practice records, electronic medical records, and our proprietary research database.
• Community Outreach: Strong partnerships with community organizations, assisted living facilities, and healthcare networks.
• Advanced Screening: Biometric scanning prevents dual enrollment and ensures subject integrity.
• Retention Strategies: Personalized follow-ups, transportation assistance, and engagement programs to maximize retention.
• Skilled CRCs: Our Clinical Research Coordinators average 8 years of trial experience, ensuring compliance and patient safety.
• Blinded & Unblinded Teams: Dedicated teams maintain study integrity.
• Regulatory Expertise: Deep knowledge of FDA, IRB, and sponsor requirements ensures strict compliance.
• Skilled CRCs: Our Clinical Research Coordinators average 8 years of trial experience, ensuring compliance and patient safety.
• Blinded & Unblinded Teams: Dedicated teams maintain study integrity.
• Regulatory Expertise: Deep knowledge of FDA, IRB, and sponsor requirements ensures strict compliance.
• High-Enrollment Studies: Consistently exceeding vaccine recruitment goals.
• Strong Industry Relationships: Trusted by leading pharmaceutical companies, and CROs.
• Diverse Participant Pool: Enhancing study impact through inclusive recruitment.
Ideal Clinical Research is dedicated to advancing vaccine development with expertise, technology, and patient-centered care.
