Jobs at Centessa Pharmaceuticals

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.

Lead nonclinical and translational strategy and operations by developing integrated timelines and plans, maintaining dashboards and metrics, coordinating cross-functional teams and CRO deliverables, preparing governance and regulatory materials, and facilitating communication to ensure program alignment and operational rigor across early-stage R&D.

The Vice President, Pharmacovigilance & Safety will provide strategic leadership in drug safety, overseeing global pharmacovigilance activities, and managing safety risk assessments and compliance across clinical development phases and post-marketing. This position involves collaboration with various teams and regulatory authorities.