Part-Time Medicines Regulatory Advisor

New Zealand Government; Wellington; On-site; NZD 210,000 - 245,000; Part time

Job summary

New Zealand Government, based in Wellington, seeks a medically qualified regulatory professional to approve medicines for New Zealanders. You will appraise clinical data, assess benefits vs risks, and advise committees on indications and safety.

The role emphasizes collaboration, critical thinking, and effective communication across teams. The position is part-time (up to 22 hours weekly) on a fixed-term basis until September 2027, pro-rated from a salary midpoint of NZD 130,470 per annum.

Qualifications

• Medical professional with registration or eligibility to register with the NZ Medical Council.
• Experience evaluating clinical trial data and regulatory information for medicines.
• Ability to communicate complex clinical concepts clearly to diverse audiences.

Responsibilities

• Assess efficacy and safety of medicines to support regulatory decisions.
• Present evidence and recommendations to expert committees.
• Identify risks and propose regulatory solutions for patient safety.
• Monitor medicine safety and contribute to pharmacovigilance.
• Mentor colleagues and ensure high-quality clinical advice across projects.

Skills

Critical appraisal

Clinical knowledge

Communication

Regulatory evaluation

Relationship building

Education

Medical qualification and NZ Medical Council registration

Job description

New Zealand Government, based in Wellington, seeks a medically qualified regulatory professional to approve medicines for New Zealanders. You will appraise clinical data, assess benefits vs risks, and advise committees on indications and safety.

The role emphasizes collaboration, critical thinking, and effective communication across teams. The position is part-time (up to 22 hours weekly) on a fixed-term basis until September 2027, pro-rated from a salary midpoint of NZD 130,470 per annum.