Overview In this CRA role, you monitor oncology/hematology trials and ensure adherence to ICH-GCP, local regulations, and SOPs. You collaborate with the Regional Clinical Operations Manager to meet study milestones and maintain data quality. You identify gaps, propose CAPAs, and support site start-up and local expertise. You work across sites to drive timely recruitment, data collection, and inspections readiness, contributing to BeOne’s mission to fight cancer. Responsabilidades * Perform feasibility, site identification, selection and evaluation to support site recruitment targets * Provide protocol and study training to sites * Conduct pre-study, initiation, routine monitoring, and closeout visits per plan and SOPs * Co-monitoring visits when required * Complete monitoring visit reports per ICH-GCP and BeOne standards * Track regulatory submissions, recruitment, CRF completion, and data queries at sites * Maintain communication with sites and report progress, issues,



and actions to Clinical Operations * Ensure inspection readiness of studies and sites * Collaborate with Regional Clinical Operations Manager and sites to deliver milestones (startup, recruitment, database analyses, closeout) * Attend disease-specific and CRA training; facilitate Study Oversight Visits (SOVs) * Evaluate site practices for quality and GCP, escalate issues as needed * Identify site issues and propose CAPA; pursue operating excellence and innovation Requisitos principales * BS in a scientific discipline plus minimum 2 years of monitoring experience * Experience in oncology general trials preferred * Understanding of clinical trial processes and ICH guidelines * 2+ years CRA monitoring experience in pharma or CRO * Excellent communication and interpersonal skills * Strong organizational, prioritization, and multi-tasking abilities * Fluency in English and Spanish (writing and speaking) * Computer skills in Word, Excel, MS Project, PowerPoint, Outlook * Travel up to 60% * communication * interpersonal skills * organization * ICH-GCP knowledge * SOP adherence * CRF data management

📌 Clinical Research Associate (Islas Baleares)
🏢 Beigene
📍 Islas Baleares