Provide research knowledge and project management skills to enable coordination/delivery of high quality research practice, inclusive of screening participant eligibility, obtaining participant consent, collecting data for identified research study/project, monitoring and reporting, and disseminating research findings. In line with Human Research Ethics Committee and Good Practice Guidelines, effectively coordinate Haematological and Oncological Clinical Trials. This role requires high level organisational, documentation, and attention to detail skills, with the ability to liaise with internal and external stakeholders.
