Our Services
Phase I-III Clinical Trials
TCR-Solutions delivers your clinical development programme end-to-end — or supports any single phase — with deep hospital-site expertise and CRA-led monitoring.
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End-to-end clinical development support
TCR-Solutions is equally happy supporting your entire clinical development programme or simply offering advice and guidance on how to optimise study set-up at a single investigative site.
We bring senior clinical, operational and biostatistics input from day one so your protocol, timelines and budget hold up under regulatory scrutiny.
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Setting up your ideal hospital partner sites
Hospital site selection is a vital component of your clinical trial’s success. Our unique, in-depth understanding of hospital people, processes and infrastructure means we are experts at selecting the very best investigative sites to achieve your project goals. Because we have detailed knowledge of hospital site people, processes and infrastructure, our project management team is ideally placed to ensure your study meets its objectives on time and within budget.
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Project management built around your study
Project Management is a key element of our clinical trial services. We begin by working with you to collaboratively develop a set of comprehensive project plans, to predict and mitigate future challenges including an in-depth Risk Analysis.
A proactive and responsive service to maximise your study’s potential — we predict, plan and adapt as the trial evolves.
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Study monitoring by experienced CRAs
Our study monitoring service is conducted by an exceptionally experienced team of CRAs with a strong background in clinical research across both hospitals and academia. Rely on our unrivalled experience for optimal study delivery — our CRAs work in partnership with site staff, providing ongoing oversight throughout the trial.
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Biometrics & Pharmacovigilance under one roof
Biostatistics, data management, statistical programming and CDISC-compliant submissions — all delivered by senior biometricians from study start.
Combined with end-to-end pharmacovigilance and medical monitoring, our integrated services keep your trial safe, compliant and decision-ready.