TARA JONES
Clinical and Regulatory Principal Consultant
Tara Jones is a Principal Consultant with over 15 years of IVD experience in regulatory and clinical affairs. With a BSc Honours in Biology and experience spanning from laboratory research to senior consulting, Tara specializes in global regulatory strategy, clinical trial management, and regulatory submissions across therapeutic areas including: infectious diseases, molecular diagnostics, and oncology. Having managed international multi-million-dollar clinical studies, Tara guides innovative diagnostic products from development through market authorization, with particular expertise in IVDR and FDA compliance. Tara has a passion for helping to navigate complex regulatory pathways for novel healthcare technologies.