Descripción de la oferta
Clinical Research Associate (CRA)Siga leyendo para descubrir lo que necesitará para tener éxito en este puesto, incluyendo habilidades, cualificaciones y experiencia.We are seeking a motivated and detail-oriented Clinical Research Associate (CRA) to join our team. The selected candidate will support the planning, monitoring, and execution of clinical studies, ensuring compliance with Good Clinical Practice (GCP), regulatory requirements, and internal quality standards.This is an excellent opportunity for growth, with on-the-job training and mentorship provided.Prepare, conduct, and report remote and onsite monitoring visits in accordance with the Monitoring Plan and applicable SOPs.Assess investigational site performance and ensure compliance with study protocol, GCP, and regulatory requirements .Perform all required activities during monitoring visits according to internal and/or sponsor procedures.University degree in Medicine, Biology, Biochemistry, Pharmacy, Nursing, Psychology, Chemistry , or other life science fields.Master's degree in Clinical Study Monitoring or an equivalent qualification.Training RequirementsKnowledge of the regulatory framework governing clinical studies.Understanding of data protection regulations applicable to clinical research.Candidates with strong interest in clinical trials will also be considered; training and mentorship will be provided .Desirable experience in clinical investigations with medical devices .SpanishAdvanced English level (spoken and written).Knowledge of established quality standards and ability to follow internal instructions. xcskxlj Familiarity with cloud-based IT platforms and digital tools.Full time positionHybrid work
