Clinical Site Manager (Continuous Glucose Monitoring)
hace 2 días
Sant Cugat del Vallès
Experteer Overview In this role you will lead and execute clinical studies at study sites, ensuring high-quality data, regulatory compliance, and patient safety. You’ll collaborate with cross-functional teams, manage site selection and activation, and oversee CRO partners to deliver trials efficiently. Your work supports Roche’s mission to diagnose earlier and personalize treatment, improving patient outcomes globally. This position offers a visible impact on product registrations and real-world evidence generation. Compensaciones / Beneficios • Act as primary site expert, coordinating training and technical support for site staff • Perform site assessments and activations, including regulatory approvals and contracting • Develop and manage site documents (informed consent, source docs, CRFs) and contribute to study protocol reviews • Oversee CROs and train CRAs, escalate issues, and mentor colleagues • Execute site management for sponsor studies across start-up, conduct, and close-out • Validate product performance claims and support regulatory submissions with data • Collaborate in local and global study teams to ensure cross-functional alignment and operational excellence Responsabilidades • Bachelor in Science (Health Sciences like Clinical Diagnostics) or engineering, or equivalent experience • Experience in Medical Device or Diagnostics clinical studies (IVD/Medical Device/Drug) • Familiarity with cardiovascular/metabolic indications and Near Patient Care or Point of Care • Strong understanding of ICH GCP guidelines for clinical trials • Ability to make decisions, analyze problems, and work in a fast-paced, matrixed environment Requisitos principales •
Fernando G.Activo hace 5 días
