
Our pre-vetted, standardized MSA and CTA framework eliminates the typical legal back-and-forth, drastically reducing review time to hit our 30-day activation target (average 90+ days industry-wide).
We submit budgets based on our internal True Cost Worksheet, ensuring accelerated financial startup and eliminating negotiation delays
Our operational model integrates eSource, eConsent, and is built to support Hybrid and Decentralized Clinical Trials (DCTs) for future-proofing your studies.
We leverage community outreach and specialized recruitment strategies in the diverse NYC/NJ metro area to help sponsors meet their enrollment goals and also specialize in recruiting underrepresented populations in clinical research.
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