We assist researchers across all stages of clinical trials, including:
- Research concept development and endorsement
- Support for grant preparation and submission
- Biostatistics and health economics modelling
- Quality of life and patient reported outcome modelling
- Facilitating active partnerships with consumer advocates and patients
- Mentoring and peer review opportunities for researchers via Discipline-Specific Advisories
- Trial budget development and management
- Trial design and protocol development
- Ethics submission and protocol compliance
- Feasibility evaluation and site selection
- Access to local and international trial recruitment networks
- Site initiation training and trial start-up
- Trial and research project management
- Data and safety monitoring
- Database build and data management
- Monitoring and data validation
- Close-out and archive