Hudson Global, Inc. invites experienced Medical Practitioners to join the Clinical Evaluation Section as MO3 Evaluators.

In this non-clinical role, you will evaluate complex clinical data and pharmacological evidence to support the approval and registration of prescription medicines on the national register. You will collaborate with multidisciplinary teams, synthesize findings into regulatory reports, and contribute to post-market review processes while ensuring compliance with Australian

A key Federal Government regulatory health body is seeking experienced Medical Practitioners to join the Clinical Evaluation Section as Medical Officer Class 3 (MO3) Evaluators. In this high-impact, non-clinical role, you will be instrumental in safeguarding public health across Australia. You will conduct critical evaluations of complex clinical trial data, pharmacological evidence, and submission packages to provide authoritative, evidence-based recommendations that guide the approval and registration of prescription medicines on the national register.

• Undertake comprehensive, evidence-based evaluations of complex clinical data and scientific dossiers submitted for prescription medicine approvals and variations.
• Formulate clear, defensible clinical assessments and risk-benefit analyses to inform high-level regulatory decisions.
• Provide expert clinical and scientific advice on safety, therapeutic efficacy, and quality.
• Collaborate with multi-disciplinary scientific teams, external expert committees, and regulatory decision-makers to meet national health standards and statutory timeframes.
• Contribute to continuous improvement in regulatory processes and the ongoing post-market review of therapeutic products.

• Recognized medical degree (MBBS or equivalent).
• Current, unrestricted registration as a Medical Practitioner with the Australian Health Practitioner Regulation Agency (AHPRA).
• Australian Citizenship is essential.

• Demonstrated experience in clinical data evaluation, clinical trials analysis, epidemiological studies, or academic research.
• Prior experience in a health authority, pharmaceutical clinical governance, or regulatory medicine environment.
• Solid understanding of the Australian risk-based regulatory framework for therapeutic goods and federal government decision-making processes.
• Exceptional written communication skills, with the ability to synthesize complex scientific findings into clear regulatory reports.

Hudson is committed to helping you find a workplace where you feel respected, supported, and free to thrive. We welcome applications from all backgrounds, identities, and lived experiences-because when different voices come together, amazing things happen

Please note for all Australian based contract and temporary roles only, the pay rate is inclusiveofmandatory 25% casual loading. This excludes permanent and fixed term roles.

Due to current Victorian labour hire licence restrictions, Hudson is not advertising, offering or accepting applications for contract, temporary or labour hire roles that are based in Victoria or otherwise connected to Victoria. This includes contract, temporary or labour hire roles where the candidate resides in Victoria, even if the role is based in another state. These restrictions do not apply to permanent or fixed term employment opportunities.