Sarah Gould

IATP satellite symposium
,

Senior regulatory pharmaco-toxicologist with extensive experience (28+) in both biotech and blue chip international pharmaceutical companies and a Contract Research Organisation, including management and leadership roles.  Held various roles, including Head of Non-Clinical and Chief Development Officer, supporting 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, with over 100 successful regulatory submissions across the globe, to support clinical trial (first in human and beyond), including BLA and MAA registrations. Also supported regulatory policy and guidelines.