CRA Level II

Clinical Research Associate (Level II) responsible for monitoring investigator sites (remote or on-site) to ensure protocol and regulatory compliance, ICH-GCP adherence, and proper documentation. Conducts site visits, data verification (SDR/SDV/CRF), inventory review, and prepares reports. Manages communications with sites and sponsors, initiates site activities, and supports risk-based monitoring, issue resolution, and audit readiness. Requires life sciences degree or RN certification, and about 1 year of relevant experience; frequent travel (60-80%) with work across office, lab, clinical, or home settings. Frequent collaboration with clinical teams, investigators, and project management; strong documentation and writing skills; proficiency with MS Office and clinical trial systems. Travel and site-management responsibilities are core to the role.