I've delivered SAS-based clinical analysis, ADaM datasets, and regulatory reporting at Cliantha Research Limited across multiple therapeutic areas.
As a Biostatistician II, I developed and reviewed ADaM specifications, datasets, output specifications, and reports for concurrent clinical trials. I also authored Statistical Analysis Plans and Clinical Study Report sections, resolved client queries, and managed sponsor audits.
Earlier at Cliantha, I generated and quality-checked Tables, Listings, and Figures against SAPs and CDISC standards, supported randomization and blinding procedures, and tracked budgets and regulatory submission timelines.
I've also worked at Cytel on SDTM CRF annotation, ADaM datasets, and laboratory shift reports. I'm a SAS Certified Base Programmer with an M.Sc. in Statistics and experience leading training, work allocation, and statistical programming reviews.
