Senior Project Officer - SAGE Trial
Position Summary
The Senior Project Officer will play a key role within the School of Health Sciences, Faculty of Medicine and Health, providing high-level project management and operational support for the Scalable Allied Health and General Practice Responses to Long-COVID in Primary Care (SAGE) Trial, funded by the Medical Research Future Fund (MRFF).
Reporting to the Chief Investigator (Senior Lecturer), the role is responsible for coordinating the implementation and delivery of primary care–based research projects, including project planning, reporting, ethics and governance submissions, study documentation, and data collection activities. Working closely with multidisciplinary teams and external stakeholders, the Senior Project Officer ensures research projects are delivered on time, within scope, and in accordance with governance, quality, and confidentiality requirements. The role has no direct reports.
Some Key Skills Required:
- Relevant tertiary qualification in clinical research with subsequent relevant experience or equivalent competence gained through any combination of education, training and experience. Experience in primary care is preferred.
- Excellent written and verbal communication skills, including interactions with diverse clinical and research stakeholders, with a high level of attention to detail for deliverables produced.
- Demonstrated success working effectively and collaboratively on initiatives with a range of people at different levels within an organization.
- Experience working with a range of computer systems and applications, including Microsoft Office suite with a proven aptitude for learning new software packages (e.g., REDCap).
- Excellent time management skills, with a demonstrated ability to respond to changing priorities, manage multiple tasks and meet competing deadlines by using judgement and initiative.
- Proven project coordination experience, with an understanding of the project life cycle and development of project plans, objectives and documentation including developing study protocols, completing ethical and regulatory applications and modifications and reporting.
- Experience with research project coordination including financial management, management of clinical data collection in Good Clinical Practice (GCP), data transfer and database development and maintenance, and data cleaning and analysis in a clinical trial context.
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