Study Design, & Biostatistics
YCCI’s Protocol Design, Development & Feasibility (PDDF) team provides methodological and biostatistical support for clinical and translational research.
Protocol Design, Development & Feasibility
The YCCI Protocol Design, Development & Feasibility (PDDF) team offers services to Investigators across the University to support Investigator Initiated research across multiple funding sources and study types. PDDF service teams can support Investigators in all stages of the research life cycle and across all types of research projects including but not limited to pre-clinical studies, early phase clinical trials, large multicenter clinical trials, behavioral research, biomarker discovery, data registries and repositories, and methodology work.
Our teams are available to meet with Investigators to discuss support services that fit your project needs. Requests for consultation and service proposals can be submitted on the service request form link.
Study Design, & Biostatistics
Clinical Trials Project Management
The regulatory landscape for Investigator Initiated research is evolving, and the administrative requirements have become increasingly more complex in recent years. The YCCI PDDF Clinical Trials Project Management (CTPM) team can help Investigators navigate these requirements and run successful studies by establishing milestone-based project timelines and tracking progress toward deliverables.Read MoreClinical Data Management
Clinical Data Managers (CDM) are critical members of your clinical trial team, working hand-in-hand with project management, study monitoring, and biostatistics to ensure that the data generated from your study are accurate and complete and that your results are reliable and meaningful.Read More