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.
Vaccines
Vaccine Research Site Capabilities
Expert Medical Team
Our board-certified Principal Investigators (PIs) and Sub-Investigators have extensive clinical trial and vaccine research experience.
Participant Recruitment & Retention
- Diverse Recruitment Channels: We access multiple databases, including private practice records, and our 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.
Experienced Clinical Research Team
- 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.
Regulatory Compliance & Data Security
- Strict SOPs & GCP Compliance: Adherence to all regulatory guidelines.
- Secure Data Management: Encrypted database systems with restricted access.
- Quality Assurance: Regular internal audits and monitoring visits. Multiple FDA audits with no 483’s
Proven Track Record
- 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.
5
Therapeutic Areas
13
Years of Experience
400
Trials Conducted
32,000
Patient Database
