Novel Clinical Research Center — Clinical Trials Miami

Advancing Medicine Through Research

A dedicated multispecialty Phase II–IV research site in Miami, FL — connecting patients, physicians, and sponsors with tomorrow's treatments.

I Want to Participate Sponsor Information Contact Us

Phase II–IV

Clinical Trials

Years Experience

Subject Database

1–2 Wks

Regulatory Startup

Who We Serve

Clinical Research That Connects

We bridge patients seeking cutting-edge treatments, physicians who want to offer more options, and sponsors who need a trusted research partner in Miami.

Patients

Access to New Treatments

Participate in clinical trials at no cost. Access investigational therapies before they are available to the general public, with close medical supervision throughout.

Apply to participate→

Physicians

Expand Your Patients’ Options

Connect your patients with active clinical trials across neurology, internal medicine, pulmonology, psychiatry, and more. Our team handles all coordination.

Contact our team→

A Site Built for Excellence

Fully equipped, dedicated facility with experienced staff, a robust subject database, and a proven track record in Phase II–IV trials.

View our capabilities→

For Patients

Why Participate?

Clinical trials offer real benefits — and our team is with you every step of the way.

Cost — compensation for time and travel

24/7

Physician on-call throughout the study

Early

Access to treatments before general availability

Expert

Dedicated team of doctors, nurses, and coordinators

What is a clinical trial?+

A clinical trial is a research study in human volunteers designed to answer specific health questions. Carefully conducted trials are the safest and fastest way to find treatments that work in people and new ways to improve health.

Does it cost anything to participate?+

No. Volunteers do not pay to participate. In most cases participants are compensated for their time and travel. All details are in the informed consent form before you begin.

Who can participate?+

Each trial has specific eligibility criteria. Our team will review your information and determine if you qualify for any active trials.

Are clinical trials safe?+

The FDA strictly regulates clinical trials to protect participants. You will receive complete information about the study and sign an informed consent document. You can withdraw at any time — participation is always voluntary.

Is my information protected?+

Yes. Your personal identity and medical information are known only to you and the research team — never shared with pharmaceutical sponsors. Results are reported only as overall trends.

How Trials Work

The Four Phases

Every approved treatment goes through this process before reaching patients.

Phase I

Safety First

Small group studies testing safety and dosing after animal testing.

Phase II

Efficacy Testing

Larger blinded, randomized studies evaluating safety and effectiveness.

Phase III

FDA Approval Path

Large-scale trials confirming effectiveness. Successful completion leads to approval.

Phase IV

Post-Market Studies

Studies on already-approved treatments for additional safety and dosing data.

Currently Enrolling

Studies That Benefit You

Participate in clinical trials at no cost — and get compensated for your time and travel. These are real studies, with real medical oversight, open to qualifying patients in Miami.

Neurology

Memory & Cognitive Studies

Studies for individuals experiencing memory loss, dementia, or Alzheimer’s disease. No cost — compensation provided.

Check if I qualify ›

Neurology

Behavioral Symptoms Studies

Studies for individuals with Alzheimer’s-related agitation — anxiety, restlessness, and aggression. Confidential, no cost, compensation for time and travel.

Check if I qualify ›

Psychiatry

Mental Health Studies

Studies for dementia-related psychosis — hallucinations and delusions. Confidential, no cost, compensation for time and travel.

Check if I qualify ›

Cost to you

Compensation varies by study. Our coordinator will confirm details at screening.

See if I qualify

Patient Enrollment

Apply to Participate

Fill out this short form and our research coordinator will contact you within 1 business day to review your eligibility.

Our Capabilities

Fully Equipped, Fully Dedicated

Laboratory Processing

Cold centrifuge and –20°C freezer for sample processing and storage.

Secured Drug Storage

Controlled access storage compliant with all regulatory requirements.

ECG Equipment

On-site electrocardiography for cardiovascular monitoring.

Monitor Workstations

Dedicated workstations with wireless internet for sponsor monitor visits.

24-Hour Physician On-Call

Around-the-clock physician availability for participant emergencies.

Our Facility

A fully staffed, dedicated research site with two exam rooms, an on-site laboratory, and a pharmacy — designed exclusively for clinical research. Strategically located near Baptist Hospital and West Kendall Hospital. No scheduling conflicts — our staff is 100% focused on active studies.

2 Exam RoomsOn-site LabPharmacyNear Baptist HealthCentral IRBCrash CartCPR Certified Staff

Therapeutic Areas

A Multispecialty Research Site

Active and prior experience across core therapeutic areas.

Neurology

Internal Medicine

Gastroenterology

Cardiology

Allergy / Immunology

Pulmonology / Respiratory

Musculoskeletal

Psychiatry

Hematology

Otolaryngology (ENT)

Nephrology

Geriatrics

Reproductive Health

Dermatology

Rheumatology / Connective Tissue

and others…

Our Space

Inside Our Research Center

Waiting area

Front desk

Exam Room 1

Exam Room 2

For Sponsors

A Partner Built for Results

From initial regulatory submission to study closure — quality, speed, and reliability.

Experienced Research Team

Diversified experience in multiple therapeutic areas. Full-time staff maintains complete focus on study requirements — source documents, CRF data, enrollment logs, drug accountability and industry standards in every study we conduct.

Robust Patient Recruitment

Allied with physicians serving the Baptist Health System of South Florida plus a proprietary database of over 1,000 potential subjects across multiple therapeutic areas.

Fast Regulatory Startup

Independent status enables use of a central IRB, shortening the approval process. One-to-two week turnaround on regulatory and contract startup — substantially faster than industry standard.

Beyond Research

Novel Clinical Research is more than a research center. We also operate as a private medical practice, delivering high-quality, and individualized patient care. This unique combination gives our patients access to cutting-edge research opportunities alongside comprehensive, personalized treatment — all under one roof.

For Sponsors

Interested in Partnering?

Tell us about your trial. Our team responds within 1 business day with a feasibility assessment.

Quality & Compliance

Built for Trust

Every standard, certification, and layer of oversight a sponsor or physician would expect — and a few more.

ICH-GCP Trained Staff

Study coordinators and investigators certified in ICH Good Clinical Practice — renewed on schedule.

Central IRB Capability

Independent status enables central IRB use — ethics approval in days, not weeks.

VCT-Enabled Screening

Voluntary Counseling & Testing integrated into screening for protocols requiring serology verification.

HIPAA Compliant Handling

End-to-end patient data handling aligned with HIPAA — secure storage, limited access, audit logs.

Direct PI Oversight

The Principal Investigator reviews every enrollment decision and adverse event personally.

CPR Certified Staff

The full clinical team maintains current BLS/CPR certification for participant safety.

“Research is how tomorrow’s standard of care is shaped today.”

Heber Varela, MD · Principal Investigator

Our Team

Experienced, Dedicated

All staff are CPR certified and trained in clinical research protocols.

Heber Varela, MD

Principal Investigator & CEO

Board Certified in Psychiatry and Neurology, Clinical Neurophysiology & Neuromuscular Medicine. Attending physician at Novel Clinical & Neurology Private Practice.

Kebir Bedran, MD

Principal Investigator / Sub-Investigator

Board Certified in Internal Medicine. Baptist treating physician.

Malú Bienes, PharmD

Pharmacist

Doctor of Pharmacy supporting investigational drug management, dispensing, and trial medication logistics.

Yakima Martínez, RN

Lead CRC

Lead Clinical Research Coordinator · Regulatory Specialist · Rater.

Anna Paula Casanovas

Site Coordinator

Clinical Research Coordinator · Rater · Patient Recruitment & Operations Coordinator.

Maite Artunedo

Site Coordinator

Clinical Research Coordinator · Phlebotomist · Medical Assistant.

Research Insights

From Our Research Center

Plain-language guides to clinical trials in Miami — what to expect, how safety works, and how to take part.

Clinical Research
Nov 2025

What to Expect When You Join a Clinical Trial in Miami

Curious about clinical trials? Here is a clear, step-by-step look at what taking part involves — from screening to follow-up — at our Miami research center.

Participant Safety
Oct 2025

Are Paid Clinical Trials Safe? How Participant Safety Works

If you are considering a paid study, safety is the first question — and a fair one. Here is how clinical trials protect participants at our Miami research center.

Eligibility
Oct 2025