Lead development of clinical data systems across LATAM (Mexico, Brazil, Argentina, Colombia, Chile, Peru).
Drive data standardization and build validation frameworks for global trials.
Design high-performance databases and ETL pipelines; mentor junior engineers.
Ensure regulatory alignment with GCP and FDA 21 CFR Part 11; maintain audit trails.
Develop dashboards and analytics to monitor data quality and trial progress.
Collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs.

🎯 Requirements

Bachelor's Degree in life sciences, statistics, data management, or related field.
Minimum 6 years experience in clinical monitoring or clinical trial management.
Advanced programming and automation skills; database design; dashboards; CDISC governance.
Professional working proficiency in English.
Excellent communication and time management skills.
Ability to mentor junior engineers.

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