
Miami Lakes, Florida
Phase II-IV research capability
Multi-specialty investigators, South Florida patient access, clinical sample processing, monitored storage, and coordinated imaging access.
View Miami LakesOne network. Two established research sites.
Wellness Clinical Research connects sponsors and CROs with bilingual, multi-specialty research teams in Miami Lakes, Florida and Vega Baja, Puerto Rico.

Choose your path
Explore site capabilities, investigators, patient access, startup support, quality, and our coordinated network model.
Why WellnessLearn how clinical trials work, what protects your safety, what to expect, and which studies are enrolling.
Explore participationRefer an appropriate patient or explore collaboration with a local research team that respects continuity of care.
Physician resourcesWhy Wellness
Both WCR sites operate within established private-practice environments, combining direct patient access and physician referral pathways with dedicated research teams and centralized coordination.
Network advantage
Place opportunities in Miami, Vega Baja, or both through one coordinated research organization.
Our locations
Each location combines dedicated research operations with access to established medical practices, local patient populations, and bilingual support.

Miami Lakes, Florida
Multi-specialty investigators, South Florida patient access, clinical sample processing, monitored storage, and coordinated imaging access.
View Miami Lakes
Vega Baja, Puerto Rico
Community-based patient access, on-site laboratory workspace, infusion and observation capability, monitored storage, and coordinated imaging access.
View Vega BajaTherapeutic expertise
Our investigator network spans gastroenterology, metabolic disease, dermatology, cardiology, pediatrics, vaccines, respiratory disease, neurology, and more.
Recruitment and retention
Established practice populations, physician referrals, community outreach, digital campaigns, bilingual call support, and consistent follow-up form the foundation of our study-specific recruitment approach.
Explore recruitment capabilitiesOperational readiness
Investigator fit, patient access, protocol requirements, and realistic enrollment potential.
Regulatory, budget, contract, central IRB, training, and activation support.
Participant-centered visits, responsive communication, and quality-focused operations.
Enrolling now
Study listings and applications are securely powered by the existing Wellness Clinical Research trial platform.
Blog & News
Meaningful Wellness milestones and practical perspectives from the clinical research site level.
A new Cochrane review challenges several common recruitment assumptions. The site-level lesson is not to abandon communication materials, but to stop treating them as a substitute for responsive, measurable human follow-up.
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FDA’s new Expedited IND Pilot explicitly encourages IRB review and site activation to proceed alongside IND development where appropriate. The opportunity is real, but only if sponsors and sites manage changing documents, financial exposure, and first-in-human readiness through clear operational gates.
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NIH is revising a proposed clinical trial application form after researchers raised questions about site readiness, multisite organization, recruitment, retention, community engagement, and inclusion. The practical lesson extends beyond grant-funded research: feasibility should be supported by operational evidence before the protocol and enrollment forecast harden.
Read moreStart a conversation
Discuss investigator fit, patient access, site capabilities, and placement in Miami, Vega Baja, or both.