Our Services
Clinical Trial Site Selection & Site Setup
From investigator identification through to site activation, TCR Solutions selects the right sites and gets them trial-ready, fast.
Site Selection & Setup
What We Deliver
We combine database intelligence with hands-on relationships to shorten your time to first patient in.
Our services include investigator and site identification using validated databases, site qualification visits (SQVs) and capability scoring.
We also provide contract and budget negotiation support, essential document collection and IMP supply readiness, site initiation visits (SIVs) and activation tracking — ensuring every site is fully prepared before the first patient is enrolled.
The Value
Why It Matters
Better site selection means faster site activation and time to first patient in, higher-quality data through sites that are genuinely capable, and reduced screen-failure and drop-out rates.
Our hands-on knowledge of hospital research departments ensures you are not relying on outdated database entries.
FAQs
Frequently Asked Questions
How quickly can sites be activated? We routinely activate sites within 8–12 weeks of selection, subject to ethics and regulatory approvals.
Do you have an existing investigator network? Yes — TCR maintains long-standing relationships with investigators across multiple therapeutic areas.