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Posted 19 hour(s) ago
Reference: 3208863798
Position classification: Medical Officer - Classification 3
Position title: Evaluator
Section name: Clinical Evaluation Section
Start date: ASAP
End date: 12 months from commencement
Possibility of extension: Up to 12 months
Hours: Part-time / Full- time (up to 37.5 hours per week)
Location: Canberra - Fairbairn, Sydney - Parramatta, Queensland - Brisbane and Melbourne
Eligibility Requirements: Australian Citizenship is essential
Background information on the BranchThe Medical Officer Class 3 (MO3) within the Prescription Medicines Authorisation Branch (PMAB) is responsible for undertaking critical evaluations of complex clinical data and evidence submitted in support of prescription medicine applications. The role provides clinical and scientific advice and prepares evidence-based recommendations to support regulatory decision-making regarding the registration and variation of prescription medicines on the Australian Register of Therapeutic Goods (ARTG).
The role contributes directly to PMAB's regulatory, operational and strategic objectives by supporting the timely assessment of prescription medicine applications, maintaining the quality and integrity of regulatory decisions, and helping ensure Australians have timely access to safe, effective and high-quality medicines.
Duties of positionThe Medical Officer (MO3) evaluator role requires highly specialised clinical expertise, the ability to critically evaluate complex clinical data and a detailed understanding of regulatory decision-making frameworks.
This role requires appropriately qualified and experienced medical practitioners.
Mandatory requirementsHold a qualification in Medicine and be registered as a medical practitioner with the Australian Health Practitioner Regulation Agency.
DesirableExperience working within a health, regulatory or scientific environment, preferably in medicines regulation.
Understanding of Australian risk based regulatory framework for therapeutic goods and knowledge of Australian Government regulatory processes.