Optimal Research Sites is an independent clinical trial facility in Central Florida with 30+ years of investigator-led research, a dedicated 9-bed Phase I inpatient unit, in-house regulatory, and a certified sample processing lab — under one operating platform, with one sponsor point of contact.
Our team has conducted Phase I–IV studies across the areas below. Earlier-phase and first-in-human studies are conducted at our dedicated Phase I unit; Phase II–IV and observational studies run out of the main site.
Protocols are matched to the right clinical specialty and surrounded by centralized ORS operational support — startup, regulatory, recruitment, and study conduct.
Emergency Medicine / Internal Medicine
Psychiatry
Internal Medicine
Internal Medicine / Neuroscience
Pediatrics
Pediatrics
Pediatric Endocrinology
Optometry
Dermatopathology
Psychiatry
Advanced Practice Investigator / Clinical Director
9-bed inpatient facility (DeBary, FL) with 24-hour medical coverage, dialysis-capable treatment beds, and separate male/female accommodations. Purpose-built for early-phase protocols that other sites have to refer out.
Dedicated regulatory team handles IRB submission, amendment management, SAE and AE reporting, and monitor support without outsourcing. Monitor visits see source documentation maintained to sponsor standards.
On-site sample lab with refrigerated centrifuges, −70°C and −20°C storage, and computerized EKG. Most protocols avoid off-site sample routing entirely, preserving sample integrity and shortening turnaround.
Central Florida location at the intersection of Orlando International and Sanford International airports. Bilingual English / Spanish team supports a demographically diverse participant base most single-site operations cannot match.
Dedicated coordinator-to-participant relationships, on-site amenities (WiFi, streaming, quiet rooms), and travel reimbursement reduce drop-out across long-duration protocols — including oncology, rheumatology, and cardiovascular studies.
Typical IRB turnaround under two weeks for amendments, with full study activation achievable inside 30 days of final protocol. GCP-trained staff ready on day one.
Send us a feasibility questionnaire or jump on a 30-minute call. We can turn around a site capability questionnaire inside 48 hours and coordinate a site visit within two weeks.