Sponsors & CROs

At NextGen Research, we believe that collaboration is the key to advancing medicine. We work closely with sponsors and CROs to design and execute clinical trials that are efficient, compliant, and patient-focused. Our mission is to accelerate drug and device development while maintaining the highest standards of data integrity, patient safety, and regulatory compliance.

We understand the demands of modern clinical trials and the importance of reliable sites that can deliver high-quality results on time. By partnering with NextGen Research, sponsors and CROs gain access to experienced investigators, diverse patient populations, and a fully equipped, research-ready facility.

Experienced Principal Investigators & Staff

Our board-certified investigators lead trials across multiple therapeutic areas. Each PI is supported by a dedicated team of research coordinators, nurses, pharmacists, lab technicians, and regulatory specialists to ensure every aspect of the study runs smoothly.

State-of-the-Art Infrastructure

We provide sponsors with a complete research environment, including:

• Fully equipped examination rooms and procedure suites
   
• Electronic data capture (EDC) and regulatory-ready systems
   
• On-site labs, imaging capabilities, and diagnostic equipment
   
• Secure storage for investigational products
   

Access to Diverse Patient Populations

NextGen Research is located in Hialeah, Florida, serving a diverse community with broad representation across age, ethnicity, and disease states. This helps sponsors achieve faster enrollment and improved retention, particularly for studies requiring specific demographics or rare patient populations.

Proven Track Record:

We have successfully conducted Phase II–IV studies, observational research, and device evaluations across a variety of therapeutic areas. Sponsors and CROs consistently highlight our timely enrollment, high-quality data, and proactive communication as major advantages of working with NextGen.

NextGen Research provides expert coverage across a broad range of therapeutic areas:

• Cardiology & Metabolic Disorders – heart failure, diabetes, obesity, hyperlipidemia
• Neurology & Psychiatry – Parkinson’s disease, Alzheimer’s disease, migraines, multiple sclerosis, schizophrenia, depression, bipolar disorder
• Dermatology – atopic dermatitis, alopecia areata, psoriasis, acne
• Respiratory & Immunology – Asthma, COPD, bronchiectasis, pneumonia, sleep apnea, autoimmune disorders
• Rheumatology – osteoarthritis, rheumatoid arthritis, psoriatic arthritis, low back pain
• Gastroenterology – IBD, ulcerative colitis, IBS, Crohn’s disease, liver disease
• Infectious Diseases & Vaccines – COVID-19, RSV, HIV, Herpes simplex, investigational vaccines
   

Each therapeutic area is managed by investigators with specialized training and experience, ensuring protocol adherence, accurate assessments, and high-quality reporting.

NextGen Research is more than a patient recruitment site—we provide full-service clinical research capabilities, including:

• Advanced Data Collection & Analysis – precise capture and monitoring of study data with robust quality control
• Expert Research Design & Methodology – guidance on protocol design, feasibility, and study optimization
• Insightful Reporting & Strategic Recommendations – clear, actionable reports to keep sponsors informed and confident
• Participant Safety & Monitoring – rigorous AE/SAE tracking and management, following FDA, ICH-GCP, and IRB standards
• Flexible Study Management – capacity for inpatient/outpatient studies, device trials, and complex interventions

By partnering with NextGen Research, sponsors and CROs can expect:

• Rapid Start-Up Timelines – Central IRB approvals, pre-qualified facilities, and regulatory expertise to minimize delays
• High Enrollment & Retention – targeted recruitment strategies and culturally competent engagement to retain participants
• Transparent Communication – frequent updates, accessible staff, and dedicated project liaisons
• Regulatory Compliance – strict adherence to ICH-GCP, FDA guidelines, and study protocols
• Tailored Solutions – flexible approaches for Phase II–IV, device, and rare disease studies

NextGen Research follows rigorous standard operating procedures (SOPs) and maintains continuous training for all staff. Our quality program includes:

• Routine monitoring of study data
• Audit-ready documentation
• Standardized participant care procedures
• Continuous improvement feedback loops
   

We aim to exceed sponsor expectations, ensuring that each study delivers reliable, actionable results.

We view every partnership as a collaborative journey. Sponsors and CROs benefit from:

• Early Feasibility Assessment – realistic recruitment projections and protocol optimization
• Customized Operational Plans – scheduling, visits, and procedures tailored to study needs
• Ongoing Support & Consultation – from study initiation through closeout, including scientific input and reporting