Medical Writer

Senior Medical Writer Supporting clinical regulatory documentation for Centessa Pharmaceuticals' neurodevelopmental asset portfolio, including orexin receptor agonists for narcolepsy and sleep disorders. Responsibilities Author and manage clinical study documents (protocols, Investigator Brochures, Clinical Study Reports) Collaborate with Clinical Development, Regulatory Affairs, Biostatistics, and other teams Oversee document lifecycle from draft to review and finalization, ensuring compliance with GCP, ICH, eCTD, and company standards Interpret complex clinical data and contribute to SOP development Requirements PhD or advanced degree in a scientific or clinical discipline 4+ years in pharmaceutical medical writing with at least 2 years in sponsor-level roles Neuroscience experience preferred Strong organizational, communication, and regulatory knowledge, including global trial submission requirements (FDA, EMA, PMDA) High-Value Clinical/regulatory writing Neurotherapeutics Sleep disorder indications Development stage (clinical) GCP/ICH compliance Cross-functional collaboration Familiarity with document management platforms (e.g., Veeva Vault) WorkSetup: not specified. #J-18808-Ljbffr