Statistical Consultancy

In conjunction with our clinical trial delivery, Resolutum Global also is now pleased to offer a statistical consulting service. This service uses the vast expertise of our biostatisticians, data managers and statistical programmers to assist in the following areas:

• Determine the scope of your trial at the concept stage.
• Feasibility of research questions and study endpoints.
• Review or develop statistical sections for your protocol/synopsis and/or CSRs.
• Advise on or undertake sample size calculations.
• Act on behalf of the sponsor as study statistician providing oversight of deliverable and timelines from CRO team for large multi-national studies.
• Post-hoc and exploratory analysis, including for conferences, journals or other scientific publications.
• Analysis of clinical trial data as your trial progresses between different phases or indications.
• Converting pre-CDISC studies into CDISC and other regulatory requirements.
• Rescue studies or review of your statistical documents, and datasets.
• General statistical/data collection and planning advice.

We are flexible and adaptable and take a pragmatic and simple approach to engagement. If you have a statistical question, please reach out, and remember it’s always better to get statistical advice before committing to a trial design, endpoint as it is often more expensive and time-consuming to retrospectively apply changes once a clinical trial has begun.