Medical Advisor

health; Wellington; On-site; NZD 70,000 - 80,000; Part time

Job summary

Manatū Hauora, the Ministry of Health in New Zealand, is seeking a medicine regulatory professional in Wellington for up to 22 hours per week on a fixed-term basis. You will review clinical trial data and other evidence to determine benefit-risk balance and advise committees.

This role emphasizes collaboration, policy impact, and safeguarding public health while offering flexible scheduling to balance family commitments.

Qualifications

• Medical qualification and be registered or eligible for registration with the New Zealand Medical Council.
• Excellent critical thinking with the ability to pull together clear ideas and conclusions from very large quantities of clinical data.
• Excellent written and oral communication with the ability to communicate complex ideas to different target groups.
• The ability to manage a dynamic workload with changing priorities.

Responsibilities

• Evaluate clinical evidence - Assess the efficacy and safety of new and existing medicines to support regulatory decisions.
• Advise expert committees - Present clinical evidence and recommendations to expert advisory committees to guide decision-making.
• Identify and address key concerns - Review medicine applications, identify potential risks, and implement clinical and regulatory solutions for better patient outcomes.
• Monitor and evaluate medicine safety - Contribute to performance monitoring, reporting, and continuous improvement of medicines regulation.
• Support team capability and communication - Mentor colleagues, review Medsafe communications, and ensure high-quality clinical advice is provided across projects.

Skills

Critical appraisal

Clinical knowledge

Written & oral communication

Workload management

Education

Medical qualification

Registered with NZ Medical Council

Job description

Wellington based | up to 22 hours per week

Fixed term until September 2027

Salary midpoint of $130,470 per annum pro-rated

Ko ake mahi - What you'll do

In this role you will be part of a team approving new medicines for NewZealanders. By using your critical appraisal skills and clinical knowledge you will evaluate the clinical trial data and other scientific information to determine if the benefits of a medicine outweigh the risks of side effects. You will also help regulate medicines in use by evaluating if new indications are acceptable and monitoring safety. Your ability to build and maintain working relationships will help you effectively make decisions that will impact public health. If you are looking for a flexible role to balance family commitments or other part time clinical roles this is the job for you.

In this role you will

• Evaluate clinical evidence - Assess the efficacy and safety of new and existing medicines to support regulatory decisions.
• Advise expert committees - Present clinical evidence and recommendations to expert advisory committees to guide decision-making.
• Identify and address key concerns - Review medicine applications, identify potential risks, and implement clinical and regulatory solutions for better patient outcomes.
• Monitor and evaluate medicine safety - Contribute to performance monitoring, reporting, and continuous improvement of medicines regulation.
• Support team capability and communication - Mentor colleagues, review Medsafe communications, and ensure high-quality clinical advice is provided across projects.

Ko pūkenga - What you'll bring

• You will have a medical qualification and be registered or eligible for registration with the NewZealand Medical Council
• Excellent critical thinking with the ability to pull together clear ideas and conclusions from very large quantities of clinical data
• Excellent written and oral communication with the ability to communicate complex ideas to different target groups
• The ability to manage a dynamic workload with changing priorities

Ko wai mātou - About us

At Manatū Hauora - Ministry of Health we are the kaitiaki of the health system, providing leadership and driving strategy and performance. We regulate the health sector and are the primary source of advice on health matters.

The Clinical Risk Management branch of Medsafe is responsible for provide advice on the clinical aspects of medicine applications, Clinical trial applications, and pharmacovigilance. We also publish Prescriber Update and provide the secretariat for the Medicines Adverse Reactions Committee.

Ko mātou me tō matou whare - What we bring

Unlock your career potential at Manatū Hauora, where you'll discover a world of opportunities for personal and professional growth. We're not just a workplace; we're a whanau that values your well-being and the importance of work-life balance. At Manatū Hauora, diversity and inclusion are woven into the fabric of our culture, ensuring that every voice is heard and every perspective matters. Your wellness is our priority, with comprehensive support and resources to keep you thriving. Join us today and be part of a team dedicated to improving healthcare.

Ngā Uaratanga - Our values

• Manaakitanga ( Listen on Māori Dictonary.co.nz ) - we show care, inclusion respect, support, trust, and kindness to each other
• Kaitiakitanga ( Listen on Māori Dictionary.co.nz ) - we preserve and maintain an environment that enables the Ministry and our people to thrive
• Whakapono ( Listen on Māori Dictionary.co.nz ) - we have trust and faith in each other to do the right thing
• Kōkiri ngātahi (Listen on Māori Dictonary.com Kōkiri + ngātahi ) - we connect and work together collectively towards a common purpose.

To apply, you must hold the right to work in NewZealand.

Applications close on midnight Tuesday 6 October.