Associate Director, Clinical Quality Assurance

Role: Associate Director of Clinical Quality Assurance overseeing GCP compliance for Centessa-sponsored early to late-phase clinical trials in neurology, focusing on narcolepsy and sleep disorders. Responsibilities: lead GCP QA programs, conduct and manage audits of investigational sites, CROs, and systems, develop audit strategies, support regulatory inspections, and ensure documentation and process adherence. Collaborate with cross-functional teams on protocol design, risk management, and training; monitor evolving GCP regulations, and lead quality improvement initiatives. Qualifications: BS or higher in Life Sciences, Chemistry, Pharmacy, with 8-10 years in pharmaceutical quality roles. Experience with document control software (e.g., Veeva Vault, ZenQMS) required. High-Value: clinical QA for GCP compliance, regulatory inspection readiness, early to late-phase trials, neurotherapeutics, in US-based role with occasional travel. Work setup: full-time, US-based, remote with travel.