The Medicines Regulation Division (MRD) is responsible for undertaking evaluations of applications to approve new medicines for supply in Australia. MRD also has responsibility for ongoing monitoring of medicines approved for supply in Australia to ensure they continue to maintain an appropriate level of quality, safety and efficacy following entry into the Australian marketplace.
The successful candidate will assist with a range of activities to support work in the Clinical Trials Team in the Risk Management Section. The Policy Analyst will support the business area in gathering data, analysing information and influencing the innovations in the clinical trial administrative procedures. They will further assist in developing policy and support project management in the team, whilst also contributing to broader work across the clinical trials sector in Australia.
Applicant Kit
Applicant Kit
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