SERVICES

Trial Management

Full end-to-end oversight that keeps your study moving—mitigating risk, maintaining quality, and harmonising every operational, regulatory and site workflow.

Why sponsors work with us

Why sponsors work with us

Agile, responsive delivery

A small, highly specialised team means faster decisions, flexible resourcing and direct access to senior experts throughout your study.

Deep operational expertise in CNS and controlled substances

Our team brings hands-on experience managing Schedule 1–4 compounds and complex psychiatric protocols across diverse trial settings.

Integrated with a high-performing site network

Close coordination with our London and NHS-embedded sites allows smoother start-up, quicker issue resolution and stronger alignment between project teams and delivery teams.

Global experience, local execution

Our project leaders and monitors have overseen studies across the UK, EU and US, bringing global standards to a focused UK delivery model.

Aligned time zones for US and EU sponsors

UK hours offer optimal overlap with both US East Coast and Europe, enabling real-time communication and rapid turnaround.

SENIOR CLINICAL TRIALS MANAGER

Rebeca James

Over 12 years’ experience working with global CROs and top ten Pharma and Biotech as a Clinical Project Manager, including Icon, Syneos Health and Iqvia. Broad range of experience in the set-up and delivery of trials from phase I-IV in Oncology, CNS and imaging.​

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