Pei Ma is an Associate Director of Data Management in Cambridge, MA with 11 years’ experience bridging clinical pharmacology, NGS-based companion diagnostics, and scalable data engineering. She has led cross-functional teams through FDA PMA/sPMA submissions and built ETL pipelines, R packages, and Shiny apps to turn complex genomic, clinical trial, and real-world datasets into auditable regulatory-grade deliverables. Her background spans hands-on PK/PD and population modeling (Monolix, NONMEM), CDISC SDTM/ADaM programming in SAS, R and Python, and web development with Django/Flask—combining deep statistical training (MS Applied Statistics, PhD Chemistry) with product-focused software engineering. Notably, she has been a core contributor to FoundationOne CDx validation and designed data platforms that integrate internal and external clinico-genomic sources for regulatory and partner use. Pei excels at translating scientific requirements into reproducible, validated pipelines and mentoring teams to maintain compliance under audit.
11 years of coding experience
13 years of employment as a software developer
Master of Science (MS) Applied Statistics, Master of Science (MS) Applied Statistics at Syracuse University
Bachelor of Science (B.S.) Pharmaceutical Sciences, Bachelor of Science (B.S.) Pharmaceutical Sciences at Tianjin University
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