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 data collection and reporting is provided to allow for quality dashboard development, collaborate with site teams 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: Based Remotely. There is also the potential for permanent employment following the initial 12-month contract period.
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.
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.
- Develop and manage dashboards and analytics tools to support trial performance and decision-making.
- Support data governance, quality assurance, and reporting across research systems.
- Collaborate with IT and research teams to deliver and maintain data products and platforms.
- Support partnerships and contribute to business development through data insights.
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.
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.
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📌 Site Research Data Analyst
🏢 Icon Group
📍 Wagga Wagga