Statistical and Data Management Support for Clinical Trials

The QSU has extensive experience collaborating on both federal and industry sponsored clinical trials where responsibilties include the following

-       Design trials (including defining endpoints and sample size calculations for interim and final analyses)

-       Create and implement statistical analysis plans

-       Design, create, and manage databases

-       Design and implement quality control procedures

-       Create randomization allocation

-       Disseminate findings through publications and conferences

-       Facilitate regulatory processes including reporting

-       Create operational reports for Executive/Steering/Clinical Endpoint Committees