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Led a statistical programming team for critical studies, ensuring no major client comments. Coordinated project deliverables within timelines and budgets, managing end-to-end activities for CRF annotations, SDTM, ADaM, and TLF creation.

Delivered global Phase II and local Phase I studies across diverse therapeutic areas. Ensured CDISC-compliant data submissions and mentored junior programmers while conducting technical trainings.

Coordinated and led the statistical programming team to deliver studies within timelines and budget. Validated ADaM datasets and created standard macros to improve team efficiency.

Led programming for SDTM datasets and supported CSR studies. Provided analysis support for Phase III clinical trials and reviewed all outputs for quality and accuracy.

Provided SAS programming for all clinical trial phases, validating CRF annotations and CRT dataset specifications per CDISC or sponsor requirements while training junior SAS programmers.

Worked closely with biometricians to generate tables, listings, and reports for FDA submissions, analyzing Phase II and III clinical trials and developing macros to streamline processes.

Completed a Master of Science in Applied Mathematics, focusing on advanced mathematical concepts and their applications in various fields.

Completed a Bachelor of Science in Mathematics, Statistics, and Computers, providing a strong foundation in quantitative analysis and computational techniques.