I support CROs, pharmaceutical companies, and medical device manufacturers through every phase of the clinical data lifecycle — from protocol and eCRF design, through data management and quality control, to statistical analysis and regulatory-compliant report writing. With an analytical background and PhD in Biochemistry, and over 15 years of combined academic and industry experience, I bring both the medical depth to understand your data in context and the technical rigour to extract clear insights from it. I work to ICH E6(R2) GCP, CDISC (SDTM/ADaM), and FDA standards.

years of experience
peer-reviewed publications
clients
projects completed