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For Sponsors and CROs

The Cardiovascular Site That Hits Your Enrollment Numbers -- and the Diversity Your Reviewers Now Demand

Senior PI is Dr. William W. O'Neill, U.S. TAVR pioneer and National PI on Edwards PARTNER, Protect II, and Protect IV. 20+ pharma sponsors. ICH-GCP E6(R3) compliant. The only dedicated cardiovascular ASC in South Florida sits 12 miles from our front door. Hispanic, Haitian, and Caribbean enrollment baked in -- your FDA Diversity Action Plan, already covered.

Trusted by Alnylam / Pfizer / Pharmacosmos / JK07 Bio / VASA Therapeutics / Cardiovascular Systems / 14 more.

Two outpatient cardiology offices in Miami-Dade plus a dedicated ASC — see locations.

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New: read our 2026 sponsor decision guide for evaluating cardiovascular trial sites →New: need a Latin America arm too? Read our cross-border strategy guide →New: FDA DAP and cardiovascular site selection →
Built-in patient flowEnrollment moatLargest independent CV practice in Miami

Powered by amavita Heart and Vascular Health® — the largest independent cardiovascular practice in Miami

Sponsors get enrollment from a continuously-recruiting cardiology practice with a high cardiovascular patient volume — not a CRO sourcing from referral networks. Our PIs see trial-eligible patients in clinic every day, screen them in real time, and convert them in the same building.

amavita Heart and Vascular Health® is the largest cardiology practice in Miami owned by a private physician (Dr. Pedro Martinez-Clark, MD, P.A.) — independent of any academic medical system. That ownership structure is the enrollment moat: in-house patient flow no competing Miami site has.

In-house

Continuous CV patient pipeline from the parent practice

No referrals

Eliminates the slow, costly CRO referral-network bottleneck

Same building

Trial conversion happens at the point of cardiology care

IAOCR GCSA CertifiedICH-GCP E6 (R3)SCRS Member

Why Amavita

Six reasons sponsors choose Amavita Research as their Miami site partner.

IAOCR GCSA Recertified May 2026

Sponsor audit prep, condensed. GCSA is the only ISO-style site accreditation in clinical research. We were recertified on 13 May 2026 (valid through 28 February 2027). Your monitor does not have to verify what an independent body has already certified. See /certifications for full scope.

ICH-GCP E6 (R3) Compliant

Already operating to E6(R3). When your protocol crosses a regulator's desk, our quality systems are not a question -- they are a footnote.

Blue-Chip Track Record

Trusted by 20+ sponsors including Alnylam, Pfizer, Pharmacosmos, JK07 Bio, and VASA Therapeutics. The same sponsors keep coming back for their second and third study with us -- that is the data point that matters.

Top-5 CV Site, Southeast US

Top-5 cardiovascular site in the Southeast US, by enrollment. The fewer competing sites in your study tier, the more your timeline depends on the ones that perform. We are one of them.

Diverse Miami Population

Hispanic, Haitian, and Caribbean recruitment baked in. With FDA Diversity Action Plans now mandatory for Phase 3 cardiovascular trials, our zip code is a regulatory moat -- not a marketing line.

Dedicated BD Contact

One contact: Nereisy Alonso, Sr CRC. Feasibility, budget, contracts, monitor access -- answered the same business day. No swivel-chair across four people on your CRO call.

Investigator ExcellenceFDA-Pivotal Device Trials

A Senior PI with a track record of FDA-pivotal device trial leadership

Our Senior Principal Investigator Dr. William W. O'Neill, MD, FACC has served as National Principal Investigator on the Edwards PARTNER, Protect II, and Protect IV trials — a track record of FDA-pivotal device trial leadership matched by few investigators in the United States.

Advanced Cardiovascular of Miami catheterization lab
Affiliated ASC · Strategic Differentiator

South Florida's only dedicated cardiovascular ambulatory surgery center

Sponsors partnering with Amavita Research gain access to South Florida's only dedicated cardiovascular ASC — enabling complex device and structural-heart studies, same-day procedures, and a controlled outpatient setting that streamlines protocol execution and reduces hospital-based variability.

3D ImagingCardiac Mapping SystemCatheterization LabsMinimally Invasive Interventional SuitesOne-Stop Diagnosis-to-Intervention Workflow
Visit the surgery center site

ASC Capabilities

Procedures supported on-site

Complex device, structural-heart, and interventional studies executed in a controlled outpatient setting — reducing hospital-based variability.

Cardiology

  • Cardiac Catheterization
  • Cardiac Mapping & Ablation
  • Coronary Intervention
  • Implantable Cardiac Monitors
  • Pacemakers / ICDs / Bi-Ventricular Devices
  • Peripheral Artery & Vein Angiography & Intervention

Interventional Radiology

  • Dialysis Access Management
  • Genicular / Hemorrhoidal / Prostate Artery Embolization
  • Kyphoplasty
  • Spinal Cord Stimulator Implantation
  • Uterine Fibroid Embolization

Technology

3D ImagingCardiac Mapping SystemCatheterization LabsMinimally Invasive Interventional SuitesOne-Stop Diagnosis-to-Intervention Workflow
Sponsor team reviewing trial dashboards

Capabilities that move your study forward

From feasibility through close-out, our team operates as a true extension of yours — bringing deep cardiometabolic experience and the infrastructure to execute complex protocols.

Therapeutic Expertise

Deep experience across cardiology, heart failure (HFrEF/HFpEF), hypertension, ACS, vascular and metabolic studies — Phase 1 through Phase 3.

Modern Recruitment Technology

EHR-integrated patient identification, predictive screening, and a digital pre-screening funnel that accelerates enrollment.

Trained, Bilingual Staff

Board-certified PI, study coordinators, and regulatory specialists fluent in English, Spanish, and Haitian Creole — matching South Florida's patient population.

Miami-Area Patient Diversity

Access to one of the most ethnically and clinically diverse patient populations in the United States.

Trusted by leading sponsors

  • Janssen
  • Pfizer
  • Alnylam Pharmaceuticals
  • Duke Clinical Research Institute
  • Pharmacosmos
  • Cardurion Pharmaceuticals
  • River 2 Renal
  • Novo Nordisk
  • Boehringer Ingelheim
  • Novartis
  • GE Healthcare
  • AngioDynamics
  • Avantec Vascular
  • Vir Biotechnology / GSK
  • Revive Therapeutics
  • CSL Behring
  • Cordio Medical
  • ImpediMed
  • Vifor Pharma
  • Salubris Biotherapeutics (JK07 Bio)

20+ pharmaceutical, biotech, and device partners — across active and completed trials

Track Record - Numbers, Not Adjectives

Performance you can underwrite

Anonymized site-level operational metrics from a 2024-active interventional vascular trial. Specific protocol disclosed under CDA.

41 days

CTA → First Patient In

Recent device atherectomy trial, 2024

32 of 39

Enrolled, on track to be first to cap

Site enrollment cap; pace-leading the trial

High retention

Through 30-day primary endpoint

Freedom from major adverse events

2–4 wk

IRB submission turnaround

Across active 2024-2025 trials

Per-protocol enrollment, screen-fail rate, and timeline data available under mutual CDA.

Sponsor Relationships

Julio G. Martinez-Clark

Chief Executive Officer (CEO)

Schedule a Sponsor Consultation

Operations & Study Coordination

Nereisy Alonso, Sr CRC

Chief Operations Officer

researchadmin@amavita.health·(786) 703-5941

Questions about how we work?

14 direct answers on PIs, timelines, capacity, certifications, cost, data ownership, and more.

Read the Sponsor FAQ

FAQ

Frequently Asked Questions

Quick answers about our certifications, leadership, and sponsor partnerships.