I’m a Principal Statistical Programmer with 10+ years of experience supporting global pharma companies with high-quality SAS programming, CDISC (SDTM/ADaM) implementation, and clinical trial analytics.
I deliver reliable datasets, TFLs, and submission-ready outputs for Phase I–IV studies.
Expert in macro development, QC, automation, and data standards.
I help teams improve efficiency, accuracy, and regulatory compliance with clear communication and top-tier technical expertise.... Mehr lesen