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. Beyond standard clinical studies, I also take on advanced clinical data-science and multi-omics projects, from spatial transcriptomics to single-cell and multi-omic data integration, bridging molecular-level data with clinical outcomes.

Photo credit: Erfan Moussavi T.
years of experience
peer-reviewed publications
clients
projects completed