Once you have your study design and concept completed, I can support your study through protocol development, through setup, planning and reporting. This may include review of any study related documents from a statistical perspective, providing guidance on selection of analysis populations and hypothesis testing, input into key data collection, statistical analysis plans, dataset specifications, statistical programming, reporting and publications. I can also assist as an independent or unblinded statistician to prepare analysis for any data monitoring committee or generate randomisation schedules.

I specialise in the implementation and reporting of studies. I am always willing to review study designs and provide feedback on the design from a statistical perspective, however I do not advise on the concept of the study and wider regulatory requirements. I would be happy to liaise with any statistical advisors involved in this early stage of design.

Please contact me with your requirements and we can work together to see how I can best support you.