• Exciting opportunity with a leading medical research institute.
• Attractive salary packaging benefits.
• Previous clinical research experience is not essential.

• Clinical assessments of research participants.
• Obtaining informed consent.
• Perform study activities as required by the protocol and regulations.
• Interpretation of laboratory results, ECG, imaging.
• Monitor and evaluate study participants for the duration of the study.
• Documentation of clinical care and research findings.

• Current unconditional AHPRA Medical Practitioner Registration.
• Knowledge of ICH/GCP guidelines, MA Code of Conduct, National Statement is desirable.

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