At PPD, I led statistical programming teams supporting clinical trial deliverables, including CDISC SDTM and ADaM datasets, tables, listings, figures, DEFINE XML, and eCTD packages for FDA and EMA submissions.
As Director of Programming, I managed 68 SAS programmers across North America, Canada, Europe, China, and the Philippines. I directed resource allocation, supported budgets and contract bids, and led initiatives improving safety-data review and study-deliverable timelines.
I've built programming processes and training across clinical pharmacology, including PK/PD analysis, NonMem datasets, CLARITY resource forecasting, SOPs, and SAS standards. I focus on developing people, managing performance, surfacing risks early, and helping teams deliver high-quality work on schedule.
