Draft, plan, review, and lead the cross-functional team in sponsor data review using J-Review and SAS listing; Perform query management with the cross-functional medical monitor on clinical operations, safety, and programming data review issues; Work with the team in preparation for DSRC and DSUR by providing the metrics reports for data entry completion for the sites; Responsible for implementing the targeted source data verification (TSDV) specification module by including the primary end points in the study; Participate in study document review, e.g., clinical study protocols, statistical analysis plans, mock tables, figures, and listing (TLF) shells. Skills: J-Review, SAS, DSRC, DSUR, and TSDV. MUST BE WILLING TO TRAVEL AND/OR RELOCATE TO WORK IN UNANTICIPATED LOCATIONS THROUGHOUT THE US.