We are seeking an experiencedClinical Research Associate (CRA)to support monitoring and site management activities across multiple studies. The role involves close collaboration with study teams, sites, and cross-functional stakeholders, with a strong commitment to patient safety, data integrity, and product quality. Supportsite start-up activities, including EC/CA submissions, contract negotiation, and essential document collection. Schedule and conduct monitoring visits according to the study monitoring plan. Identify and report compliance issues, working with project management to ensure timely resolution. Ensure monitoring reports are finalized within 28 days of each site visit. Provide interim site management services, including remote monitoring, as required. QualificationsPrior CRA experience (on-site and remote) within medical devices or pharma (ISO *:****, ICH-GCP). Proactive, detail-oriented, and committed to patient safety and quality standards. ? This opportunity offers involvement inmultiple excluively sponsor studies, exposure to a wide range of clinical operations, and the chance to work in a dynamic, high-quality environment. #

📌 Clinical Research Associate (Madrid)
🏢 Oxford Global Resources
📍 Madrid