Teams at Centessa Pharmaceuticals

Lead cross-functional program management for high-complexity global R&D programs: maintain integrated program Gantt as single source of truth, identify/manage interdependencies and risks, run team meetings, maintain dashboards, issue logs and budgets, manage vendors, support regulatory submission documents, and prepare governance/executive materials while refining PM best practices.

Lead small-molecule analytical development across early-to-late stage programs, oversee CDMO/vendor analytical work, design/execute method development, validation/transfer, manage stability programs, review analytical data and regulatory sections, support investigations and batch record reviews, and coordinate domestic/international shipments.