Responsibilities include coordinating clinical research studies of varying size and complexity; identifying and screening eligible participants; coordinating recruitment, enrollment, informed consent, study visits, surveys, interviews, and other protocol-required procedures; and facilitating communication among investigators, clinical providers, research staff, participants, laboratories, and other departments. The Clinical Research Coordinator (CRC) will work independently or with general direction at the fully operational journey level to execute, manage, and coordinate clinical research activities within a federally funded Hemophilia Treatment Center (HTC) at UCSF, under the direction of the Clinical Research Manager (CRM), Principal Investigator (PI), and/or other designated leadership.