Established patient access
Both sites are embedded in private practices, with access to large patient populations, physician relationships, and connected EMR data to support protocol-specific feasibility.
Sponsors & CROs · Why Wellness
Private-practice patient access, informed feasibility, and dedicated research teams. Connect with one organization for study execution in Miami Lakes and Puerto Rico.
Startup timing is measured from receipt of a complete startup package and varies by study requirements, approvals, and sponsor or vendor readiness.
Why Wellness
Local clinical relationships, supported by a research organization that connects the people and work behind each study.
Both sites are embedded in private practices, with access to large patient populations, physician relationships, and connected EMR data to support protocol-specific feasibility.
Investigators assess therapeutic fit, patient suitability, and the clinical requirements of each protocol, helping the team identify practical considerations before study placement.
Central coordination connects investigators, local site teams, and our dedicated recruitment team, aligning study requirements, responsibilities, and follow-up across both locations.
Assigned responsibilities and responsive communication help the team address questions, coordinate next steps, and follow through as study requirements and operational needs change.
Connected by design
Evaluate Miami Lakes, Puerto Rico, or both through one organization. Connected EMR data, investigator input, and centralized recruitment support inform the review.
Our centralized team coordinates recruitment planning, patient outreach, and follow-up alongside each local research team.
Explore placement options
Both sites combine private-practice patient access with connected EMR data. Clinical and recruitment teams use this information to evaluate protocol requirements and recruitment potential across the network.
Final placement is confirmed through protocol-specific feasibility.
Working with Wellness
A productive site partnership depends on how information, decisions, and follow-up move between people.
Connect with our team
We review the opportunity with the proposed investigator and relevant teams, identifying fit, requirements, and questions that need follow-up.
Central coordination connects the clinical and operational teams, with responsibilities identified for the work ahead.
When a study requirement or operational barrier needs attention, the relevant team members are brought into the discussion and follow-up.
Explore our approach
Take a closer look at the resources and processes most relevant to your study.
Facilities, equipment, procedures, and specialty access.
Protocol assessment, recruitment planning, and activation.
Patient access, outreach, and participant follow-through.
Standardized SOPs, document tracking, training, and quality review.
Connected study information and coordinated operations.
Meet the clinicians supporting our research network.
WCR case studies
Explore eleven real studies spanning enrollment above forecast, strong screening conversion, sponsor audit results, and full participant completion, supported by preparation, participant relationships, and open communication.
Phase 3 vitiligo: 15 randomized against a forecast of 8. Sponsor audited with zero findings.
Phase 1/2 influenza immunization: 47 randomized in one month; all 47 completed approximately a year of participation and follow-up.
Phase 2 celiac disease: 8 randomized against a forecast of 6. All 8 completed, including diary, gluten-challenge, and visit requirements.
Phase 2a ulcerative colitis: first screening within 3 weeks, zero screen failures, and 100% completion.
Phase 2b cardiovascular: first screening in 43 days from selection. Five in the initial group subsequently randomized.
View individual study results across dermatology, metabolic disease, cardiovascular research, gastroenterology, neurology, and vaccines.
Start a conversation
Share your study opportunity. Our team will review fit and follow up with you.