About This Opportunity

Step into a pivotal role at the forefront of infectious diseases research, where your expertise will help shape the delivery of impactful, multi-centre clinical trials. As a Senior Clinical Trial Coordinator within the Frazer Institute, you will join a highly collaborative and purpose-driven research environment, partnering with leading investigators and stakeholders to translate innovative discoveries into real-world health outcomes. This is an opportunity to contribute to meaningful, life-changing research while mentoring others and strengthening the integrity and performance of clinical trial delivery.

Key responsibilities will include:

• Lead coordination and delivery of clinical trials, including design, setup, and ongoing study management.
• Prepare and manage key study documents (protocols, ethics/governance submissions, databases, reports, presentations).
• Serve as central communication point between trial managers, sites, and committees, providing regular updates.
• Oversee trial operations such as site initiation, monitoring visits, trial master files, and milestone tracking.
• Ensure compliance with GCP, ethical standards, and regulatory requirements.
• Drive quality improvement, maintain confidential data systems, and support ongoing enhancement of trial processes.

About You

You are a highly organised and motivated clinical research professional who thrives in complex, fast-paced environments and is driven by purpose and quality. Your ability to balance operational excellence with collaborative leadership will see you succeed in this role.

You will also have:

• Relevant degree in Science/Health (e.g., Nursing) or equivalent experience, with strong background coordinating clinical trials across the full lifecycle.
• Proven ability to work effectively in complex, fast-paced clinical and research environments.
• Solid knowledge of research methodologies, data management, and clinical trial regulatory requirements.
• Demonstrated success coordinating multidisciplinary teams and delivering on project milestones.
• Strong communication and interpersonal skills, with ability to build relationships across diverse stakeholders.
• Highly organised with strong planning, time management, and technical skills (e.g., Microsoft Office, TEAMS, REDCap), and experience managing multiple trials, including multi-centre (national/international) studies.