Feasibility & startup
Realistic feasibility. Coordinated startup. Fewer avoidable delays.
WCR centrally reviews study opportunities with the proposed investigator and applicable operational teams to determine fit across Miami, Vega Baja, or both.
Discuss Your ProtocolFeasibility assessment
Focused on what will determine study success
Our team provides coordinated feasibility assessments centered on investigator fit, patient access, recruitment potential, operational requirements, and realistic enrollment projections.
Investigator Fit
Specialty alignment, relevant clinical background, therapeutic experience, and investigator interest.
Patient Access
Practice populations, referral pathways, target demographics, and study-specific recruitment potential.
Operational Fit
Protocol complexity, procedures, equipment, staffing, timelines, and location suitability.
Startup pathway
Coordinated activities from selection to activation
Opportunity Review
Confirm study fit, proposed investigator, site placement, and preliminary recruitment potential.
Startup Package
Coordinate essential documents, regulatory requirements, training, and vendor readiness.
Parallel Review
Contract and budget review may proceed alongside regulatory startup to reduce avoidable delays.
Activation
Coordinate final approvals, translations, training, systems, supplies, and readiness for first participant activity.
Central IRB
Experienced regulatory coordination
Our team has extensive experience coordinating central IRB submissions and study-related regulatory requirements across both locations.
Have a study opportunity?
Share the protocol number, indication, phase, target population, proposed timeline, and location preference. Our team will review fit and respond directly.
Submit a Study