The Senior Principal Technical Data Specialist will define and govern enterprise technical data expectations across clinical programs in Latin America, oversee database design and EDC platform architecture, lead testing/validation and migration/archival practices, and drive integration, interoperability and AI enablement. The role is remote for Argentina, Brazil, Colombia, Mexico (and the description also references Chile and Peru) and typically requires 12+ years of relevant experience.

Lead development and optimization of clinical data systems and ETL pipelines for global trials across LATAM. Responsibilities include enterprise data standardization and mapping, designing validation frameworks, SAS-based modular codebases, database design and optimization, dashboarding, and ensuring regulatory compliance with GCP and FDA 21 CFR Part 11. Requires professional working proficiency in English and at least 6 years of relevant clinical trial/monitoring/management experience.