Lead, Clinical Data Standards & SDTM Reporting

Abb Vie is seeking a Manager, Clinical Data and Reporting Standards (CDARS) to drive the development and governance of data and reporting standards across Abbvie's clinical trial portfolio. The role emphasizes SDTM/ADaM design, SDTM programming, and documentation for regulatory submissions. The candidate will lead cross-functional teams to define data collection, review rules, and trial-level reporting displays, while ensuring consistency with eCRF and CDISC standards.