Services · Clinical research
Clinical trial design and analysis.
We help you plan, run, and evaluate clinical trials so the results are valid, reliable, and ready for the review they will face.
What is involved
Trial statistics starts long before the data arrives. We work with you on the design itself: the question the trial must answer, the sample size and power to answer it, and the statistical analysis plan that fixes the methods before unblinding.
Once data flows, we run the interim and final analyses to the plan, and report them so investigators, sponsors, and reviewers can follow every step.
What we take on
- Sample size and power calculations
- Statistical analysis plans, including mock table shells
- Interim and final analyses following the SAP
- Service as independent statistician for data monitoring committees
- Writing and review of the statistical sections of protocols
Who this is for
Pharmaceutical companies developing new treatments, medical-device manufacturers running clinical evaluations, and academic researchers conducting investigator-led trials.
The standard we work to
- Methods fixed in advance and documented, so the analysis is defensible
- Regulatory requirements observed at every stage
- Timelines honoured; trial milestones do not wait
- Reporting that both statisticians and clinical teams can read
Planning a trial, or already underway?
Tell us where the study stands and what it needs to show. We will lay out the statistical path.