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. We combine database intelligence with hands-on relationships to shorten your time to first patient in.

Clinical Research Organisation UK

What we deliver

Investigator and site identification using validated databases
Site qualification visits (SQVs) and capability scoring
Contract and budget negotiation support
Essential document collection and IMP supply readiness
Site initiation visits (SIVs) and activation tracking

Why it matters

Faster site activation and time to first patient in
Higher quality data through better site selection
Reduced screen-failure and drop-out rates

FAQs

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.

Phase I-III Clinical Trials

Real World Evidence

Investigator-initiated studies in China

Study Feasibility & Consultancy

Site Selection & Setup

Protocol Design

Regulatory Affairs

Project Management

Study Monitoring

Biometrics

Pharmacovigilance

Medical Monitoring

Start the conversation

If you are considering clinical trial support as part of your development strategy, TCR Solutions would be pleased to discuss how our services could support your programme.

Contact us info@tcr-solutions.com