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.
Capabilities
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.
Therapeutic Fit
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.
Work With Delta
Bring your protocol to Tampa Bay
Send a protocol synopsis or feasibility questionnaire and our team will respond within 48 hours.