Why Join RMH?
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Part time ongoing | 48 hours per fortnight
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Newly created role due to the growth of the Sponsor department within the Office for Research
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Support commercial trials and collaborative research in a CRA role with a difference
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Career progression opportunities to suit your professional development goals
About the role
The Royal Melbourne Hospital Office for Research is seeking an experienced Clinical Research Associate (CRA) looking for a flexible, permanent part-time role, while continuing to develop their career in clinical research. You will help shape and deliver our strategic plan and support the continued growth of our Sponsor services.
Working within an established and growing team of subject matter experts, you will support commercial and non-commercial clinical trials and research across RMH, the Parkville Precinct and throughout Australia. You will work across multiple therapeutic areas, collaborating with clinical research teams, stakeholders and commercial clients to deliver best-practice monitoring in today’s research framework.
Unlike traditional CRA roles, this position offers exposure across the full clinical trial lifecycle, including study start-up, sponsor oversight, governance, quality systems, investigator support and monitoring activities. You'll have the opportunity to partner with research teams, influence best practice and help shape the future growth of RMH's Sponsor Services program
This is an opportunity to build your career in clinical research while contributing to Precinct-wide infrastructure improvement that benefit our patients and community and supporting high-quality trial delivery within a complex and evolving ICH-GCP R3 clinical research environment.
Key Accountabilities
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Lead sponsor monitoring activities including site initiation, interim monitoring and close-out visits, both on-site and remotely.
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Ensure studies comply with approved protocols, essential documents, GCP, regulatory requirements and relevant procedures.
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Support study start-up, feasibility, site selection and Site File maintenance.
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Monitor recruitment, data quality, query resolution, safety reporting and site performance throughout the study lifecycle.
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Provide clinical operations advice, training and ongoing support to investigators, study teams and research departments to stay ‘Inspection and audit-ready’.
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Apply a risk-based approach to sponsor oversight and monitoring, identify opportunities for improvement and build strong stakeholder relationships.
About You
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Minimum two years’ experience as a Clinical Research Associate (CRA), with experience monitoring commercial clinical trials.
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Current Good Clinical Practice (GCP) certification, with strong knowledge of the compliance environment for research; ISO 14155 knowledge desirable.
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Sound understanding of the National Statement, ethics and research governance requirements.
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Strong attention to detail, with excellent communication and stakeholder engagement skills.
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Collaborative, approachable and customer-focused, with a commitment to delivering high-quality research support and enablement.
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Ready to take the next step in your clinical research career.
Benefits of Working at RMH
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Enjoy great employee benefits
Salary packaging of up to $12,000 tax free and generous leave entitlements, including additional annual leave.). -
Meaningful Work
Make a real difference in the lives of patients, families and our community. -
Career Growth
Access clinical research subject matter experts, learning, development, and diverse career opportunities. -
Supportive Culture & Belonging
Join in a diverse and values-led organisation built on kindness, collaboration and inclusion. -
Innovation
Help shape the future of healthcare through research, technology and new models of care. -
World-Class Excellence
Work alongside leading healthcare professionals at one of Australia's premier public hospitals, within the Parkville Precinct—one of the world's leading biomedical and research precincts. -
Work in the Parkville Precinct
Work in the Parkville precinct with excellent public transport, onsite parking options and access to staff health services and a variety of clinical research stakeholders.
Interested?
Click Apply to review the full job description and to submit your application, please include a cover letter and resume.
Interviews may commence as applications are received. Early applications are encouraged as the role may close once filled.
Our Commitment
We acknowledge the Traditional Owners of the lands on which we work and are committed to fostering a culturally safe environment for Aboriginal and Torres Strait Islander peoples.
As a child safe organisation, RMH are committed to the safety, wellbeing, and inclusion of children and young people, in line with the Child Safe Standards
We are proud to be a workplace that champions diversity, inclusion and equality for our staff and communities we support, we welcome applications from people of all backgrounds, identities, and abilities, and will provide reasonable adjustments throughout the recruitment process.
All appointments are made subject to satisfactory background and compliance checks, including a Criminal History Record Check (or equivalent), Working with Children Check and Immunisation assessment.
