
Study Coordinator - ISAAC
- Clayton, VIC
- Contract
- Part-time
- Recruiting and consenting participants
- Supporting participants throughout the study
- Managing data collection and entry into REDCap
- Preparing and maintaining essential study documentation, ethics, and governance submissions
- Monitoring study progress and ensuring compliance with Good Clinical Practice (GCP), ethics approvals, and privacy legislation
- A relevant degree in Science, Nursing, or related field (or equivalent experience in clinical trials)
- Knowledge of TGA/ICH/GCP guidelines, ethics, and governance processes
- Strong skills in data collection and electronic data capture systems (e.g., REDCap)
- Ability to conduct participant consent process with empathy and professionalism
- Excellent organisational and problem-solving skills