Lead, Clinical Data Standards & SDTM Reporting
Listed on 2026-10-07
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IT/Tech
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.
Consider building your career as a Lead, Clinical Data Standards & SDTM Reporting at Abb Vie.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Irvine, CA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 140..
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