If you need consultation on your study design or development, our Clinical Research Navigator can help. We will review your protocol (pre-IRB submission or following IRB-required modifications before resubmission) and offer feedback designed to help you address in advance any potential regulatory or compliance concerns such as the approach, interventions, use of regulated products, statistical methods used or design issues, record-keeping, required reporting or recruiting or consenting subjects.

If your project needs more specialized expertise in statistics, bioinformatics or clinical design, we will locate those services for you. Our goal is to serve as your “single point of contact” at FSU in finding and delivering what you need at any point in the life cycle of your research. From conception and planning to study implementation, analysis and publication of research outcomes, our goal is to facilitate your successful navigation of FSU’s research resources.

Request a consultation today so we can help you get started.