Education/Experience/Skills: Position requires a bachelor's degree in a physical science, life science, or health-related field such as biology, chemistry, or nursing and at least 8 years of experience coordinating, authoring, and editing protocols, IBs, CSRs, and other clinical regulatory documents in a pharmaceutical company or CRO environment supporting submissions to U.S. and/or EU health authorities. Our focus is developing high-potential XmAb bispecific T-cell engagers and additional engineered drug candidates that leverage our differentiated technology platforms, and we are advancing our pipeline toward clinical proof-of-concept decisions.