- Critically and systematically approach the field of Clinical Trials, analysing the contribution of each phase to the development of evidence-based medical knowledge and evaluating their methodological validity.
- Integrate principles of research ethics, bioethics, and regulatory frameworks into the design and implementation of research protocols, ensuring scientific integrity and the protection of research participants.
- Independently design research proposals, formulating original and clinically relevant research questions supported by a systematic review of the international scientific literature.
- Develop comprehensive research protocols, including methodological design, sample size calculation, selection of appropriate statistical methods, and identification of potential methodological limitations.
- Analyse and interpret complex research data, applying contemporary statistical approaches and critically assessing the reliability and generalisability of findings.
- Produce original scientific work capable of contributing to the international scientific dialogue through the preparation of manuscripts for peer-reviewed journals or presentations at scientific conferences.
- Establish the foundations for further research or doctoral study, acquiring the methodological and academic skills required to pursue PhD-level education.