Senior Scientist, Safety Assessment & Toxicology Data Analytics

Role: Senior Scientist within Safety Assessment at Centessa Pharmaceuticals, focusing on non-laboratory toxicology data analysis and strategy. Responsibilities: lead data visualization and analytics of multi-dose toxicology studies, audit SEND datasets from CROs for regulatory compliance, conduct mechanistic literature reviews to assess safety risks, and support cross-functional collaboration with Toxicology, DMPK, CMC, and Project Development teams. Influence early pipeline decisions and contribute to regulatory submissions. Requirements: B.S. or M.S. in Toxicology, Pharmacology, or related sciences; 6–8+ years (M.S.) or 8–10+ years (B.S.) experience in biotech/pharma toxicology or data management; expert understanding of preclinical toxicology datasets, SEND data validation, and data visualization tools (e.g., Python, R, GraphPad). Preferred: strong scientific writing and cross-disciplinary communication skills, experience with regulatory safety datasets. High-Value: focus on neurotherapeutics (narcolepsy, sleep disorders), nonclinical safety, regulatory compliance, and cross-functional data integration. Work setup: remote US-based role with occasional travel.