I am a Senior Statistical Programmer with 14+ years of experience in Clinical SAS programming.
I provide high-quality, regulatory-compliant deliverables for clinical trials, including:
SDTM & ADaM dataset creation
TLF programming (Tables, Listings, Figures)
QC, validation & CDISC compliance
Support for FDA/EMA submissions
I have strong experience working with global pharma and CRO teams and can support short-term or long-term project requirements.