Clinical research built for
careful execution.
Delta Clinical Research supports Phase II-IV protocols in Tampa Bay with physician-scientist leadership, disciplined operations, and participant-first communication.
What the site is built to support
The strongest sponsor relationships start with clear feasibility, realistic enrollment expectations, and tight protocol conduct.
Phase II-IV Execution
Protocol conduct, participant visits, safety monitoring, and sponsor communication for mid- and late-stage clinical trials.
Physician-Scientist Oversight
Direct investigator leadership from Panos E. Vasiloudes, MD, PhD, board-certified in pediatrics with decades of clinical practice.
Participant Recruitment
Community-centered screening workflows for Tampa Bay participants, with clear education before informed consent.
Regulatory Discipline
Study startup, IRB coordination, documentation, and protocol adherence built around FDA and ICH-GCP expectations.
Sponsor Feasibility
Protocol review, site-capability assessment, enrollment planning, and practical startup conversations for sponsors and CROs.
Participant Retention
Coordinator-led communication, visit reminders, and plain-language support to help participants stay informed and engaged.
Protocol areas we can evaluate
Therapeutic-area pages describe capability and protocol fit. They are not a guarantee that a specific trial is currently enrolling.
CNS & Neurology
Clinical research capabilities for neurologic and central nervous system protocols in Tampa Bay.
Metabolic & Endocrine
Clinical trial site capabilities for metabolic and endocrine research across the Tampa Bay community.
Cardiovascular
Cardiovascular clinical research capabilities for Phase II-IV protocols in Tampa Bay.
Ophthalmology
Ophthalmology and vision-related research capabilities for sponsors and Tampa Bay participants.
General Medicine
General medicine clinical research capabilities for community-based Phase II-IV trials in Tampa Bay.