Role Summary
Hands-on migration of clinical trial data/documents to Veeva, including source-to-target mapping, transformation, cleansing, loading, and reconciliation.
Experience with regulated clinical platforms such as CTMS/eTMF/EDC and migration controls covering audit trails, metadata, data integrity, and GxP/21 CFR Part 11 expectations.
Experience executing mock/test/production migration cycles, handling migration defects, and supporting validation/UAT and cutover for business-critical clinical systems.