Haematology Biobank Research Coordinator (Health Manager Level 1)

Employment Type: Temporary Full Time; 38 hours per week up to June 2027 with the possibility of extension
Position Classification: Health Manager Level 1
Remuneration: $1,750.25 - $2,328.48 per week + Superannuation
Location: Royal Prince Alfred Hospital
Requisition ID: REQ690866

About the Role

You will be working at Royal Prince Alfred (RPA) Hospital. It is one of the nation’s most respected hospitals, with a distinguished history of serving the health needs of local, statewide, national and international communities. Our facilities and services are world class and our staff are dedicated, innovative and caring.

The Haematology Research Unit at RPA Hospital is seeking a motivated and detail-oriented Coordinator to play a key role in the development and ongoing management of our Haematology Biobank.

Working closely with a dedicated multidisciplinary team of clinicians, nurses, and laboratory scientists, you will contribute to a broad range of clinical research activities. Your responsibilities will include maintaining accurate documentation and patient confidentiality, supporting patient recruitment and consent processes, processing and managing biospecimens in a laboratory environment, coordinating ethics and governance submissions, liaising with a range of internal and external stakeholders, and maintaining the research database through data entry, reconciliation, and quality monitoring.

This is an exciting opportunity to develop your career in clinical research while gaining valuable experience across clinical, laboratory, governance, and data management functions. You will make a direct contribution to the growth of in-house research within the RPA Haematology Department, while working alongside a highly collaborative team committed to advancing haematology research and improving patient care.

If you are ready to take the next step in your clinical research career and join a highly respected team at the forefront of haematology research, we would love to hear from you. Join us in supporting excellence in both patient care and research.

Please note: This position is advertised until 30 June 2027. The role forms part of an ongoing program of work within the unit, with contracts renewed annually, subject to performance and ongoing program requirements. 

For more information, please view the Position Description.

Ideal Candidate

• Good working knowledge and understanding of medico-legal, privacy and ethical requirements for research as per the ICH-GCP.
• Knowledge and experience in clinical research including secure data management, participant trial data collection, skills in coordinating trial participants, ability to rapidly master new concepts and skills, detailed knowledge of HREC and RGO submissions.
• Has relevant qualifications and/or experience in research, clinical trials, or relevant clinical or other health experience.