Quality & Compliance Officer

Quality & Compliance Officer – Part-Time 12 Month Fixed Term Contract – Remote Working Arrangement

Join Icon Research in a pivotal quality-focused role supporting the oversight, compliance, and governance of clinical trials across our expanding research portfolio. This role plays a key part in ensuring trial documentation, processes, and systems meet regulatory standards and internal policies.

• Strategic Quality & Governance Role: Lead and support quality assurance activities, internal audits, SOP development, and compliance tracking across multiple trial sites. Collaborate with investigators, research teams, and external stakeholders to uphold excellence in clinical trial conduct.
• Career Impact: Be part of Australia's largest private cancer clinical trials program, with opportunities to influence research quality systems, contribute to governance frameworks, and support continuous improvement initiatives.
• Part-Time 12 Month Fixed Term Contract: This role is primarily remote, working 3–4 days per week with flexibility around which days and hours. There is also potential for ongoing permanent employment following the initial 12-month contract.

These positions attract strong interest from highly qualified candidates, so we encourage you to submit your application promptly to ensure full consideration. Take the next step in your research career and apply today.

Is this the opportunity for you?

We're seeking applicants with tertiary qualifications in health or science, and experience in clinical trial coordination, quality assurance, or governance. If you're passionate about clinical research and committed to maintaining high standards of compliance and safety, we'd love to hear from you.

About Icon Research

Icon Group operates Australia's largest private cancer clinical trials program, with a growing global footprint. We collaborate with over 200 partners including CROs, commercial and non-commercial organisations, and service providers. Our trials span Phase I–IV in medical oncology, haematology, radiation medicine, and investigator-initiated studies. To learn more, please visit

About the Role

Reporting to the Global Research Governance Manager, you'll work closely with the Global Research Implementation & Quality Manager and site-based teams to ensure clinical trials are conducted in accordance with ICH GCP, national frameworks, and Icon policies.

Key Responsibilities:

• Monitor and report on compliance across trial documentation and processes
• Support internal audits, vendor audits, and CAPA tracking
• Assist in SOP and policy development and implementation
• Provide training on GCP, governance, and quality systems
• Support risk assessments and mitigation strategies
• Prepare sites for regulatory inspections and monitoring visits
• Contribute to governance reporting and continuous improvement initiatives

About You

You're a proactive and detail-oriented professional with a strong understanding of clinical research quality systems. You'll bring:

• Tertiary qualifications in a health or scientific field
• Minimum 5 years' experience in clinical trial coordination or quality roles
• Knowledge of GCP and Australian research regulations
• Strong organisational and interpersonal skills
• Excellent written and verbal communication
• Proficiency in Microsoft Office and document management systems

These positions attract strong interest from highly qualified candidates, so we encourage you to submit your application promptly to ensure full consideration.

Excited to Join Us?

If you meet the above criteria and have an interest in quality and compliance, please directly apply now and attach your resume and cover letter to your application.

Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees. We encourage applications from all diverse backgrounds.

Learn more about Icon Research & our South Brisbane Centre

Pre-employment Health RequirementIcon is committed to managing the risk of transmission of specified vaccine preventable diseases (VPDs). Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs.