Sarah Gould

ESTP Congress
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Senior regulatory pharmaco-toxicologist with extensive experience (28+) in both biotech and blue chip international pharmaceutical companies, as well as a Contract Research Organisation. Held various roles, including Head of Non-Clinical Departments and Chief Development Officer. Supported various development programs globally from Discovery to License, across diverse drug modalities, including small, large molecules (mAbs, bispecifics, peptides, proteins), gene therapy, Oligo/RNA products and vaccines/adjuvants, with large regulatory experience; over 100 successful regulatory submissions across the globe to support clinical trials (first in human and beyond) and/or BLA and MAA registrations.  Supported regulatory policy and guidelines. Keen interest in the future of toxicology and the paradigm shift in safety assessment.