Topic: regulatory strategy

Lead global chemistry, manufacturing and controls regulatory strategy for small-molecule and monoclonal-antibody medicines. The role oversees investigational and marketing submissions, manufacturing-change assessments and health-authority interactions, working with process development, analytical development and quality teams from early development through commercialisation.

Lead the medical and clinical development strategy for Beam’s metabolic disease franchise. The role shapes clinical plans and study protocols for base editing therapies, oversees ongoing trials and patient safety, and coordinates clinical and regulatory strategy. Responsibilities include mentoring physicians and clinical scientists and working with research teams on subsequent therapeutic programmes. This hybrid role requires residence within commuting distance of Cambridge, Massachusetts.