Before investing time, money, and resources into a clinical trial or evaluation, you need certainty that your study is scientifically robust, operationally achievable, and highly impactful.
I provide independent, expert feasibility assessment and protocol development to determine whether a research proposal is viable, saving you from costly protocol amendments or premature trial closure down the line.
I provide an evaluation of your proposed project across three core areas:
Evidence gap
Working with the clinical needs you have identified, I analyse current NHS workflows to target exactly where evidence is lacking. This process builds the strong justification required to secure funding and advance your project.
Study design
I formulate clear, focused research questions and pair them with appropriate study design and practical methodologies. I incorporate robust patient involvement and engagement from the onset, ensuring the patient voice shapes the project design.
Operational validity
I evaluate target populations, clinical settings, and recruitment strategies to ensure your project’s overall viability. This process identifies potential barriers and prevents disruptions to your project timeline.
Once your feasibility assessment is complete and the study protocol is finalised my involvement can conclude. However, if your project has the funding to proceed, I can also take the lead on your study set-up phase. Find out how I manage participant materials, data systems, and regulatory packages by visiting the study set-up page.