About Vida Clinical Research

Multi-Specialty Clinical Trial Site Advancing Healthcare Through Data-Driven, Ethical Research

Vida Clinical Research is a multi-specialty Phase II–IV clinical trial facility headquartered in Kissimmee, Florida, operating under NIH, GCP, and FDA-compliant frameworks. Founded in 2019, our mission is to accelerate medical innovation while upholding the highest standards of patient safety, data integrity, and operational excellence.

As a site management organization (SMO), we work across therapeutic areas to generate high-fidelity clinical data for sponsors, CROs, and investigators.

Our Facilities

Our primary research center is located in Kissimmee, Florida, just steps away from AdventHealth Hospital. Designed specifically for clinical excellence, our facility is equipped with:

2 dedicated research exam rooms

A CLIA-certified lab

Ambient and refrigerated centrifuges

–20°C and –70°C freezers with temperature monitors

Electrocardiogram (ECG)

An FDA-secured, temperature-controlled IP storage room

All equipment is calibrated using best-in-class calibration services

Our location ensures patients have quick access to emergency care — with the nearest hospital less than 0.01 miles away.

A Network of Trusted Investigators

We work with a diverse network of physicians who are passionate about contributing to the future of medicine. Our investigators conduct trials across multiple specialties and are committed to maintaining the highest research and ethical standards. We welcome physicians and clinical experts to join our growing network. If you're interested in becoming an investigator site, contact us today.

Capabilities That Drive Results

We specialize in streamlined, rapid startup and enrollment without compromising on quality. Our proven processes are supported by:

A research database of pre-qualified patient candidates

Strong integration with multi-specialty practices

Experience across major systems including EDC, IVRS, IWRS, and ERT

Ongoing web-based sponsor protocol training

Our team’s focus on data accuracy and protocol compliance ensures that sponsors receive clean, reliable data — fast.

Quality Assurance & Oversight

With over 75 years of combined experience, our staff provides:

Site Quality Management

Investigator Recruitment

Site Selection & Study Start-Up

Regulatory Submissions & Maintenance

Monitoring of Phase II–IV Clinical Trials

SOP Creation & Revision

Risk Management & Resolution Strategies

At the heart of Vida Clinical Research is an unwavering dedication to quality management. Our oversight model follows NIH, GCP, and FDA guidelines — ensuring that every study is conducted with precision, ethics, and care.

Trusted by the Industry's Best

We’ve proudly collaborated with global leaders in pharmaceuticals and clinical operations, including:

Pfizer, Medpace, Salix, Eli Lilly, AstraZeneca, Takeda, Ardelyx, Forest, Abbvie, Quintiles, Amgen, Boehringer Ingelheim, and many others.

Expert Team. Certified Excellence.

Every staff member at Vida Clinical Research is trained and certified to uphold the highest standards of safety and performance. Our certifications include:

CRC (Certified Clinical Research Coordinator)

NIH Human Subjects Protection

CITI Training

IATA (for specimen transport)

CPR (Emergency Preparedness)