Site Research Data Analyst

Site Research Data Analyst – Full-Time 12 Month Fixed Term Contract – Remote Working Arrangement

Join Icon Research in a key data-focused role supporting the accuracy and integrity of clinical trial data across our national and international network. This role is central to ensuring timely and compliant data entry, query resolution, and reporting for oncology trials conducted at Icon Cancer Centres.

• Data-Driven Clinical Research Role: Ensure accurate and timely data entry, support query resolution, and contribute to trial documentation and reporting. Collaborate with site teams, sponsors, and CROs to uphold data quality standards.
• Career Impact: Be part of Australia's largest private cancer clinical trials program, with opportunities to contribute to research excellence and continuous improvement in data management practices.
• 12 Month Full-Time Fixed Term Contract: This role is primarily a remote working arrangement. 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.

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. Learn more by visiting

About the Role

You'll report to the Site Research Manager and work closely with clinical trial coordinators, investigators, and external stakeholders. Your focus will be on data entry, query resolution, and supporting documentation for oncology trials.

Key Responsibilities:

• Accurate and timely data entry into electronic data capture (EDC) systems
• Develop and manage dashboards and analytics tools to support trial performance and decision-making.
• Lead data governance, quality assurance, and reporting across research systems.
• Collaborate with IT and research teams to deliver and maintain data products and platforms.
• Build partnerships and contribute to business development through data insights.
• Support team training and continuous improvement in data management practices.

Is this the opportunity for you?

We're seeking applicants with tertiary qualifications in health or science, and experience in clinical trial data entry and management. If you're passionate about clinical research, have a keen eye for detail, and meet the following Key Requirements, we'd love to hear from you.

About You

We're looking for a detail-oriented and organised professional who's passionate about clinical research and committed to maintaining high standards of data quality. You'll ideally have experience in clinical trial data entry and management, along with strong communication skills and a collaborative mindset.

Key Requirements:

• Tertiary qualifications in a health or scientific field
• Experience with clinical trial data entry and resolving data queries
• Solid understanding of Good Clinical Practice (GCP) and relevant research regulations
• Strong organisational and communication skills
• Proficiency in Microsoft Office and electronic data capture (EDC) systems

Excited to Join Us?

If you meet the above criteria and want to make a meaningful impact in clinical research, please apply now with your resume and cover letter.

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

Icon is committed to managing the risk of transmission of vaccine preventable diseases (VPDs). Certain roles may require evidence of vaccination or immunity.

Learn more about Icon Research