Teams at Korro Bio, Inc.

Leads clinical data management for global clinical studies from startup through database lock and archival. Oversees CROs, vendors, EDC builds, data cleaning, external data transfers, validation, database quality, regulatory compliance, and study budgets. Develops data management plans and related documentation, supports audits and regulatory submissions, and partners with clinical, statistical, pharmacovigilance, regulatory, and operations teams. Contributes to departmental standards and process improvements.

Leads global, multicenter early-phase clinical trials from planning through closeout, ensuring compliance with GCP, regulations, budgets, and timelines. Oversees CROs, vendors, study teams, sites, monitoring, patient enrollment, clinical data integrity, safety reporting, TMF management, inspection readiness, and study documentation. Partners cross-functionally on trial strategy, protocol development, regulatory requirements, clinical reports, and risk management. Requires strong leadership, communication, strategic thinking, and experience with rare diseases, first-in-human studies, and global clinical operations.