Senior Clinical Data Manager

Role: Senior Clinical Data Manager supporting Centessa's neuro-focused early-phase programs, including orexin receptor 2 (OX2R) agonists for sleep disorders. Responsibilities: lead global clinical data management activities, develop and oversee data strategies, manage data systems (e.g., EDC, IRT, ePRO), ensure standards compliance (CDISC/CDASH), oversee CRO/vendor collaborations, and support regulatory submissions. Qualifications: Bachelor's or Master’s degree, 6+ years' clinical data management experience in pharma/biotech, expert in clinical trial technologies, experienced with CRO/vendor oversight, and familiar with regulatory requirements (Pre-IND to NDA/BLA). Preferred: experience in early-phase CNS or neurodegenerative trials, and supporting regulatory submissions. HighValue: CNS/neuro indications, early-phase (Ph1-3), global development, electronic data systems, CRO/vendor management, regulatory support. WorkSetup: based in the US, with occasional travel.