On successful completion of the Graduate Certificate in Clinical Research students will be able to
- Understand the key activities to be undertaken to ensure successful clinical trial initiation and management
- Comprehend clinical trial regulations and appreciate the importance, practical use and evolution of these regulations.
- Participate in programmes of clinical research that comply with the highest national and international legal, regulatory and scientific standards
- Be familiar with the documents required to be compiled for an ethics & regulatory clinical trial application & appreciate the important of quality system and SOPS
- Appraise, evaluate and enhance clinical research protocols, ensuring the highest quality research outputs
- Possess excellent communication and presentation skills, appropriate to the multidisciplinary clinical research environment
- Collaborate with patients, academic partners and industry to complete clinical research programmes
- Commit to continuous lifelong learning and further diffusion of their clinical research expertise