Built for Efficient Study Execution.
Novum Research conducts Phase II–IV clinical trials from our dedicated Central Florida research site, combining experienced investigators, integrated specialty partnerships, broad patient access, and technology-driven recruitment to support studies from startup through closeout.
90%
Retention rate
1-3 Weeks
IRB submission from a complete package
24 Hours
Serious adverse event reporting
1-2 Weeks
Budget and contracting
One Site. One Team. Efficient Execution.
Our feasibility team evaluates opportunities quickly and provides sponsors and CROs with clear, realistic assessments of patient access, investigator fit, operational capacity, and startup timelines.
- Experienced investigators across internal medicine, gastroenterology, cardiology, endocrinology, dermatology, and pulmonology.
- Dedicated research operations team supporting feasibility, startup, regulatory, recruitment, coordination, and study execution.
- Integrated physician and specialty partnerships providing access to diverse patient populations across Central Florida.
- Technology-driven recruitment combining EHR-based identification, AI-assisted prescreening, digital outreach, and community recruitment.
- Centralized site operations designed for responsive communication, efficient startup, and consistent study delivery.
Built to Support Complex Clinical Trials
Novum Research supports Phase II–IV studies across internal medicine, gastroenterology, cardiology, endocrinology, dermatology, pulmonology, and other therapeutic areas.
Rapid Feasibility
Fast, realistic assessments of investigator fit, patient availability, site capacity, and enrollment potential.
Multidisciplinary Investigators
Experienced investigators and specialty physicians across multiple therapeutic areas, supporting both focused and complex protocols.
On-Site Laboratory & Clinical Capabilities
On-site specimen collection and processing, centrifugation, refrigerated and frozen storage, ECG, vital signs, and other protocol-required assessments.
Investigational Product Management
Secure, temperature-monitored storage with continuous monitoring, alarm notification, backup power, and documented accountability.
Extensive Patient Access
Integrated physician networks, specialty partnerships, direct EHR access, patient databases, and targeted recruitment across Central Florida.
Experienced Research Staff
GCP-trained research professionals experienced in regulatory, recruitment, study coordination, safety reporting, data management, and protocol-specific procedures.
Inside Our Research Site
A dedicated clinical research facility designed to support participants, investigators, and complex study protocols.
Three Dedicated Clinical Trial Rooms
Private research spaces equipped for study visits, clinical assessments, and protocol-required procedures.
Clinical Assessment Capabilities
On-site ECG, vital signs, pulse oximetry, phlebotomy, and other common protocol-required assessments.
Emergency Preparedness
Emergency response equipment and supplies are maintained on site, with BLS-certified clinical staff available during study visits.
Secure Research Records
Controlled access to research records and secure electronic systems designed to support GCP, HIPAA, and study-specific requirements.
How We Execute Studies
IRB & Regulatory Startup
Central IRB experience and streamlined regulatory workflows support efficient study activation and startup.
Informed Consent
A documented consent process gives participants time to understand the study, ask questions, and make an informed decision before study procedures begin.
Safety Reporting
Adverse events and safety information are documented, assessed, and reported according to protocol, sponsor, IRB, and regulatory requirements.
EDC & ePRO
Experienced with leading sponsor-provided EDC, ePRO, eCOA, IRT, and other clinical trial platforms.
Remote Monitoring
Secure remote access to source and regulatory documentation supports efficient monitoring and reduces dependence on on-site visits.
CTMS, eSource & Regulatory
eClinPro provides integrated CTMS, eSource, electronic regulatory documentation, eConsent, recruitment, and study-management workflows.
Budgets & Contracts
Dedicated operational oversight supports responsive budget review, contract negotiation, and study startup.
Quality Management
Standardized SOPs, quality-control processes, staff training, and study-level oversight support inspection-ready documentation and protocol compliance.
Recruitment That Converts. Retention That Lasts.
Novum Research combines direct patient access, physician referrals, EHR-driven identification, AI-assisted prescreening, and targeted outreach to identify qualified participants across Central Florida.
Once enrolled, participants are supported through proactive follow-up, appointment reminders, flexible scheduling, education, and transportation assistance when needed.
300,000+
Patient population accessible through our physician and specialty networks
Multiple Referral Channels
Internal medicine, specialty practices, community outreach, and direct recruitment
AI + EHR Prescreening
Technology-assisted identification and prescreening of potential participants
Multi-Therapeutic
Established recruitment capabilities across GI, cardiometabolic, dermatology, pulmonology, and other indications
Submit a Study Opportunity
Share your study with our team for a prompt assessment of investigator fit, patient access, site capacity, and operational feasibility.
- Jovani Rivera, Site Director and Business Development
- [email protected]
- (352) 558-8655
- 290 Citrus Tower Blvd, Suite 102, Clermont, Florida 34711