Medical Officer (Clinical Research)

Join Nucleus Network as a Medical Officer and help advance medicine while building a rewarding career in clinical research.

As the world's leading Phase 1 clinical trials specialist, with facilities across Australia, the USA, and the UK, we partner with global pharmaceutical and biotechnology companies to help bring new medicines to patients.

Why Join Nucleus Network?

Work with purpose and contribute to the development of medicines that have the potential to improve the lives of people worldwide.

Ask better questions and find smarter ways of working in an environment that values innovation and continuous improvement.

Start here, go further with exposure to the full clinical trial lifecycle and opportunities to develop your career.

Be visible at scale in a global organisation where your contribution is recognised.

Grow in a growing place , with expanding operations creating new opportunities across the business.

Join a culture of curiosity where learning, collaboration and new ideas are encouraged every day.

Access benefits include Fitness Passport, Reward Hub discounts, wellbeing initiatives, recognition programs and EAP support.

About the role

The Medical Officer is a key member of Nucleus Network’s Medical Operations team, responsible for ensuring the safety and wellbeing of clinical trial participants while providing medical oversight and contributing to the successful delivery of Phase 1 clinical trials.

In this role, you will conduct medical assessments, monitor participant safety, provide clinical care, and collaborate with multidisciplinary teams to support the development of innovative new therapies.

Working alongside experienced multidisciplinary teams, you will gain exposure to all aspects of early-phase clinical research while playing a key role in participant safety, medical oversight and the development of new therapies.

Build a long-term career with opportunities to progress into Principal Investigator, Medical or Operational Leadership. You'll be supported through ongoing learning and development, mentoring, and the potential to pursue certifications to further enhance your expertise.

Key responsibilities

Leading the informed consent process and conducting medical assessments to determine participant suitability for clinical trials.

Monitoring the health and wellbeing of trial participants throughout study participation.

Providing medical care and clinical oversight to healthy volunteers and patients involved in Phase 1 studies.

Reviewing, interpreting and signing off diagnostic test results and other clinical data.

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