13+ years in pharmaceutical marketing and patient engagement, with experience across global pharma, biotech, and clinical settings, specialising in omnichannel strategy and data-driven growth.
10+ years in CMC analytical development, specialising in biologics and gene therapies, including monoclonal antibodies and viral vectors, within GLP/GMP environments.
12+ years in bioinformatics, specialising in NGS pipelines, HIV sequence analysis, and genomic data processing across clinical and research applications.
20+ years at the FDA, reviewing 260+ INDs and 20+ NDA/BLAs, with deep expertise in regulatory toxicology and CNS drug development.
15+ years in biopharma, supporting drug development from R&D to commercial manufacturing across CMC and regulatory.
