ClinicalQualityIntern

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. ### ### The Position **Main tasks and duties:** * Support Roche clinical studies and play a role in the development of new diagnostic tests, helping to ensure the quality and safety of our products. * Perform quality review of clinical study documents (study protocols, investigator brochures and * reports) to ensure that clinical studies of IVDs are planned, conducted, and documented in * compliance with regulations, internal procedures and product specification documents. * Support GCP inspection readiness activities, including through study file reviews. * Support team initiatives, including process improvement/harmonization. * Support project teams with Good Clinical Practice expertise. **Additional tasks, duties and responsibilities:** ● Additional tasks as required. **Requirements:** * Preferred Education: Recent graduates from University degree or Master in scientific or technological discipline, ideally in Biomedicine, Biotechnology field. * No previous experience needed. * Fluent command of English. * Interest in clinical studies, medical devices, quality management systems and software development processes. Knowledge of quality and regulatory standards is a plus but not * mandatory: Good Clinical Practice (GCP), ISO 13485, ISO 20916, * FDA QSR, IVDR, GDPR * This position is only available for candidates who have never worked in a company in Spain or used a "contrato de prácticas" before. **Who We Are** At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. W