About Vital Care Research

Rigorous science, delivered with care.

For over a decade, our Miami-Dade center has helped sponsors bring therapies to life — combining operational excellence with a genuine commitment to the communities we serve.

Our mission

Science that reaches
the patients who need it.

We exist to accelerate safe, effective treatments, bringing tomorrow's medicine to South Florida's diverse population today.

From first feasibility call to final close-out, our team treats sponsor data and patient wellbeing as inseparable priorities.

Clinician taking a patient blood pressure
What guides us

Principles behind every study.

01

Data integrity

Accurate, source-verified, audit-ready documentation on every visit — without exception.

02

Patient dignity

Informed, supported, and respected participants who stay engaged through study completion.

03

Operational rigor

Disciplined timelines, proactive communication, and protocols executed exactly as written.

04

Community access

Bringing trials to underrepresented populations so research reflects the patients it serves.

Exam and monitoring room
Our facility

Purpose-built for clinical research.

Our Miami site is equipped to support complex protocols end-to-end, on-site.

  • Private exam & monitoring rooms with dedicated source space
  • On-site processing, ambient & frozen sample storage
  • Temperature-monitored, access-controlled drug storage
  • Secure, redundant EDC and electronic source systems
Tour our space

A look inside our Miami facility.

Our team

Experienced people behind the data.

Board-certified investigators and credentialed research staff who have run hundreds of trials together.

Principal Investigator

Principal Investigator

MD · Board-Certified

Leads protocol oversight, medical eligibility, and participant safety across all active studies.

Clinical Research Director

Clinical Research Director

Site Operations

Owns feasibility, start-up, and day-to-day site performance against sponsor timelines.

Lead Study Coordinators

Lead Study Coordinators

CCRC · Bilingual

Manage visits, source documentation, and the participant experience from screening to close.

Credentials & compliance

Held to the highest standards.

ICH-GCP
Good Clinical Practice
FDA 21 CFR
Part 11 Compliant
IRB
Central & Local Ready
HIPAA
Privacy Safeguarded
Work with us

Let's talk about your next trial.

Get in touch