Medical Officer Class 3 (MO3) Clinical Evaluator - AHPRA registration required

Effective People

Melbourne

Hybrid

AUD 179,000 - 186,000

Full time

2 days ago
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Job summary

Effective People seeks a Medical Officer Class 3 (MO3) Clinical Evaluator for a 12-month labour-hire contract with extensions possible. Hybrid work across multiple locations, including Melbourne, ACT, NSW, QLD. AHPRA-registered medical practitioner with Australian citizenship is essential.

Role involves evaluating clinical data for medicines regulation and providing evidence-based recommendations. Flexible part-time/full-time arrangements and pay rate of $130–$135 per hour (including super)

Qualifications

  • Critically evaluate complex clinical data and evidence.
  • Apply clinical expertise to detailed evidence reviews.
  • Provide clear clinical or scientific advice based on evidence.
  • Prepare evidence-based recommendations for regulatory decisions.
  • Understand regulatory decision-making frameworks for clinical evaluation.
  • Hold a qualification in Medicine and current AHPRA registration as a medical practitioner.
  • Australian citizenship is essential.

Responsibilities

  • Critically evaluate complex clinical data and evidence submitted with prescription medicine applications.
  • Apply specialised medical expertise to regulatory assessments.
  • Provide clinical and scientific advice to support regulatory decisions.
  • Prepare clear, evidence-based recommendations for medicine registration and variation decisions.
  • Apply regulatory decision-making frameworks to complex clinical evidence.
  • Support timely assessments while maintaining quality and integrity.

Skills

Clinical data review
Clinical expertise
Regulatory reasoning
Evidence-based decisioning

Education

Medicine degree

Job description

Medical Officer Class 3 (MO3) Clinical Evaluator - AHPRA registration required

Medical Officer Class 3 (MO3) Evaluator - Health & Regulatory
Location: Fairbairn, ACT; Parramatta, NSW; Brisbane, QLD; Melbourne, VIC
Contract: Labour-hire contract, 12 months from commencement, with extension of up to 12 months
Pay: $130 - $135 p/h including super (negotiable)
Work type: Part-time / full-time, up to 37.5 hours per week
Work arrangement: Hybrid, with specific arrangements agreed with your supervisor on a case-by-case basis
Clearance: No security clearance required; Australian citizenship is essential

About the Role
This is a specialist medical evaluation role with our Federal Government client, supporting national prescription medicines regulation.

You will critically evaluate complex clinical data and evidence, provide clinical and scientific advice, and prepare evidence-based recommendations for regulatory decisions. Your work helps maintain the quality and integrity of decisions affecting access to safe, effective and high-quality medicines.

What You'll Be Doing

  • Critically evaluate complex clinical data and evidence submitted with prescription medicine applications
  • Apply specialised medical expertise to clinical regulatory assessments
  • Provide clinical and scientific advice to support regulatory decisions
  • Prepare clear, evidence-based recommendations for medicine registration and variation decisions
  • Apply regulatory decision-making frameworks to complex clinical evidence
  • Support timely assessments while maintaining quality and integrity
What You Bring (Essential Criteria)
  • You can critically evaluate complex clinical data and evidence
  • You can apply specialised clinical expertise to detailed evidence reviews
  • You've provided clear clinical or scientific advice based on evidence
  • You've prepared evidence-based recommendations that support formal decisions
  • You understand regulatory decision-making frameworks relevant to clinical evaluation
  • You hold a qualification in Medicine and current AHPRA registration as a medical practitioner
  • You're an Australian citizen
Nice to Have (Desirable Criteria)
  • Experience in a health, regulatory or scientific environment, preferably medicines regulation
  • Understanding of Australia's risk based regulatory framework for therapeutic goods
  • Knowledge of Australian Government regulatory processes

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