Clinical Trials Assistant
On-site · Nedlands, Western Australia, Australia
Job Summary
Coordinate patient bookings and activities for the Clinical Trials Unit; assist in screening patients and collecting patient history and lab results for trials; support site visits and sponsor-related requirements; coordinate ordering of supplies and monitoring of stock for trial lab kits and consumables; assist with maintaining Site Files and data entry, including resolving queries; ensure data supplied to sponsors is accurate and matches source documentation; maintain timely communication with stakeholders and build strong working relationships with clinicians involved in clinical trials at the hospital.
Required Qualifications
- Registered Nurse, allied health or science qualification
- Knowledge of Good Clinical Practice (ICH-GCP) requirements
- Prior experience in a research or clinical environment, including experience in the conduct and coordination of clinical trials would be highly desirable, particularly experience in oncology and/or haematology trials
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