Description
Centessa Pharmaceuticals is hiring an Associate Director, Study Operations Manager - Nonclinical Toxicology to manage end-to-end operations for toxicology and safety pharmacology studies conducted with external CROs. The role oversees study forecasting, budgeting, planning, data management, quality assurance, compliance, communications, and coordination with toxicology, DMPK, CMC, bioanalytical, project management, regulatory, and senior management teams. It requires a BSc or MSc in toxicology, pharmacology, or a related discipline, at least six years of biotechnology or pharmaceutical experience, and strong scientific, organizational, communication, and data-management skills. The position is full-time, exempt, remote in the United States with occasional travel, and offers a base salary of $150,000 to $220,000 plus a discretionary annual bonus and comprehensive benefits.
