Summary
Exciting opportunities available now with the Townsville Hospital and Health Service.
About the work unit / facility
The Research Coordinator for the Clinical Trials Multi‐Specialties Team at Townsville University Hospital will play a key role in supporting the establishment and conduct of clinical trials in accordance with the National Health and Medical Research Council, Good Clinical Practice Guidelines, and International Council for Harmonisation standards.
About your new employer
Supportive Workplace Culture and Regional Advantage
Our community‐driven culture fosters collaboration, inclusion, and professional support. We balance metro‐level healthcare opportunities with a regional feel, offering short commutes, access to rural and urban facilities, and a close‐knit professional network.
Work/Life Balance and Lifestyle Benefits
Nestled within beautiful North Queensland, the rural, urban, country and coastal locations across the Townsville HHS region provide vibrant communities, affordable living, stunning landscapes, outdoor adventures and a relaxed lifestyle. The region prioritises employee wellbeing, offering flexible work arrangements, stable job security and a family‐friendly environment.
Competitive salary and benefits
* Hourly rate: $47.18 to $51.98 p.h. (AO4)
* 4 to 6 weeks annual leave with 14%-17.5% loading
* 12.75% employer contribution to superannuation
* Plus Salary Sacrificing options may be available
About your opportunity
The incumbent will contribute to the research team led by a nominated Principal Investigator and the Clinical Trials Manager, while developing research expertise through involvement in defined projects relevant to a specific service group within the Townsville Hospital and Health Service.
Requirements
* Ability to comply with organisational policies and procedures, including those relating to confidentiality, information security and workplace health and safety.
* Possession of a current Good Clinical Practice Certificate, or willingness to obtain within two months of commencement.
* Highly Desirable:
o Experience providing research or clinical trials support within a healthcare or medical research environment.
o Experience coordinating or overseeing processes within a research team.
o Well‐developed organisational and administrative skills with strong attention to detail.
o Proficiency in Microsoft Office applications and familiarity with research/administrative systems (e.g., REDCap, Ethics Review Manager).
o Knowledge of legislative, regulatory and governance requirements relevant to clinical trials and health research.
o Ability to work independently and as part of a multidisciplinary team.
o A relevant qualification in administration, business, health administration or a related discipline would be well regarded.
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