At Ephicacy Consulting Group, I served as lead programmer across oncology and medical device studies, defining programming strategy and aligning deliverables with regulatory submissions. I built SAS macros to generate standard tables and co-led fast-turnaround projects, including work to recover at-risk deliverables.
At IQVIA and earlier CROs, I programmed and validated CDISC SDTM/ADaM datasets, Define-XML, reviewer’s guides, and TLFs for clinical trials and regulatory submissions. I’ve mentored statistical programmers, presented at PharmaSUG, and worked across therapeutic areas including pain management and oncology.

