Genetics Research Coordinator
Quick Summary
Part-time (14 hours per week) fixed term opportunity until 31 July 2027,
About the Role
~2 min readAn exciting opportunity exists for a Genetics Research Coordinator to join a dynamic research team based at the Charles Perkins Centre and contribute to the Australian Type 1 Diabetes National Screening Research Program.
Working closely with Dr Kirstine Bell, the Research Manager and research team at the Charles Perkins Centre, as well as a national multidisciplinary network of researchers, clinicians and stakeholders, you will provide critical support to the delivery of an MRFF-funded project on polygenic risk screening for type 1 diabetes. You will play a key role in the coordination and implementation of research work packages across collaborating institutions, including recruitment and participant engagement across projects, operational planning and research activities in hospital and community settings. You will also contribute to ethics and governance processes, grant reporting, internal and external communications, and the organisation of research meetings and events. Opportunities may also be available to support laboratory-based research activities and data analysis.
This is a unique opportunity to contribute to a nationally significant research initiative that aims to transform the early detection and care of type 1 diabetes in Australia. You will join a collaborative and supportive research team delivering meaningful public health impact for children and families, while enjoying genuine flexibility in how and where you work.
Responsibilities
~1 min read- →coordinate the delivery of the research program across collaborating institutions and project work packages
- →develop and maintain effective relationships, clinicians industry and community partners, sponsors and another key stakeholders
- →support the end-to-end delivery of various research activities, including study start-up, participant coordination, data collection, and close-out activities
- →maintain accurate clinical trial documentation and data records in accordance with regulatory, ethical and Good Clinical Practice (GCP) requirements
- →prepare and coordinate ethics and governance submissions, grant reporting requirements, and compliance activities
- → coordinate reporting activities, monitor data integrity and support compliance initiatives across clinical research projects
- →manage purchasing, invoicing and payment processes related to research activities
- →contribute to risk management, protocol review activities and continuous improvement initiatives that support a strong safety culture
- →facilitate communication across a broad range of stakeholders to support successful research outcomes and participant engagement.
- a bachelor's degree in a relevant discipline, or an equivalent combination of training and experience
- demonstrated experience supporting or coordinating clinical trials within a research, health, academic or public health environment
- knowledge of ICH Guidelines and Good Clinical Practice (GCP) requirements
- experience coordinating ethics submissions, research governance activities, or regulated research programs
- experience maintaining accurate records, managing research data, and producing reports
- strong organisational skills with the ability to manage competing priorities across multiple stakeholders and projects
- excellent written and verbal communication skills, including the ability to engage effectively with researchers, clinicians, schools, community groups, and healthcare stakeholders
- experience working with schools, community organisations, healthcare providers, or research participants will be highly regarded
- demonstrated attention to detail and commitment to quality, compliance, and ethical research practices
- proficiency using research-related systems, databases, and standard business software applications.
To keep our community safe, please be aware of our COVID safety precautions which form our conditions of entry for all staff, students and visitors coming to campus.
Sponsorship / work rights for Australia
You must have unrestricted work rights in Australia for the duration of this employment to be eligible to apply. Visa sponsorship is not available for this appointment.
Requirements
~1 min readApplications (including a cover letter, CV, and any additional supporting documentation) can be submitted via the Apply button at the top of the page.
For employees of the University or contingent workers, please login into your Workday account and navigate to the Career icon on your Dashboard. Click on USYD Find Jobs and apply.
For a confidential discussion about the role, or if you require reasonable adjustment or any documents in alternate formats, please contact Danielle Selinger Recruitment Consultant by email to danielle.selinger@sydney.edu.au
Location & Eligibility
About this job
- Pay per year
- $93,345 a year
- 30% above the $71,888 median for Research Associate jobs on Jobera (478 salaries).
- Posted
- 2 days ago
Listing Details
- Posted
- November 13, 2026
- First seen
- November 13, 2026
- Last seen
- November 14, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 63%
- Scored at
- November 14, 2026
Signal breakdown
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