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Clinical Trial Coordinator
part-timeCamperdown

Summary

Location

Camperdown

Type

part-time

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About this role

  • Part time one year contract available

  • A chance to work with the MRFF funded AUS HEARTS project- adapting and implementing an evidence-based approach to blood pressure management in regional and remote NSW

  • Base Salary starting from $103,185 + 17% superannuation 
     

About the opportunity

The university is seeking to employ a Clinical Trial Coordinator ( HEO 6) to join Dr Niamh Chapman, Senior Research Fellow and team in the MRFF-funded multidisciplinary research project - AUS HEARTS. The AUS HEARTS project will adapt and implement the World Health Organization's HEARTS approach, which has been successfully used in over 30 countries, to the unique context of regional and rural Australia. The project will focus on Western NSW, where hypertension rates are 10% higher than the national average.

The primary goal of the AUS HEARTS project is to improve the detection and management of hypertension, to reduce the risk of heart attacks and strokes in rural communities. By providing a simple and standardised approach for busy primary care clinics, the project aims to ensure that more people receive effective treatment for high blood pressure.


The AUS HEARTS project is committed to improving cardiovascular health in regional and rural areas through community collaboration, team-based care, and strategic partnerships. It involves working closely with local communities and health services to adapt the HEARTS program to their specific needs, using multidisciplinary healthcare teams to identify and manage high blood pressure. The project involves a broad network of investigators and partner organisations including the Royal Flying Doctor Service, local pharmacies and general practices, and several national peak bodies. The research aims to implement HEARTS and evaluate how effective this approach is for managing hypertension in regional Australia.

The Clinical Trials Coordinator will support AUS HEARTS clinical trial processes, from planning to execution, ensuring a seamless transition through all stages. They handle data capture, verification, and overall adherence to standards while fostering relationships with research staff and stakeholders.

The incumbent will be located within the Susan Wakil Health Building located on the Camperdown campus.

Full‑time employment may be considered for applicants who show exceptional suitability for the role.

Your key responsibilities will be to:

  • Support the end-to-end clinical trial process, assisting with the planning, initiation, and execution of trials, and ensuring smooth operations from start-up to close-out

  • Support data capture and verification for clinical trials, maintaining accurate records and ensuring compliance with regulations

  • Follow ethics guidelines and workplace health and safety regulations, preparing materials for committee submissions

  • Build productive relationships with research staff, trial sponsors, and external vendors, facilitating effective communication and collaboration

  • Uphold the principles of Good Clinical Practice (GCP) in all clinical trials, ensuring that ethical and scientific quality standards are met in design, conduct, recording, and reporting

  • Take the lead in handling stakeholder communications, ensuring that concerns are addressed effectively and timely while fostering a culture of trust and collaboration within the work area and beyond

  • Facilitate timely report submission, uphold data integrity according to university systems, and partner with managers to advance compliance initiatives

  • Coordinate purchasing processes and resolve any discrepancies in payment schedules

  • Champion a proactive approach to health and safety, review and provide feedback on work area protocols, and collaborate cross-functionally to ensure consistent safety standards across tasks and projects.

About you

  • Bachelors degree in relevant field or equivalent combination of relevant training and experience

  • Experience in clinical trial coordination or a similar role

  • Solid understanding of clinical research and Good Clinical Practice

  • Experience with ethics and governance processes and preparing and submitting trial documentation

  • Effective communication, planning and organisation skills and strong attention to detail

  • Proven experience in a research-intensive environment.

Sponsorship / work rights for Australia

Work Rights: you must have unrestricted work rights in Australia for the duration of this employment to apply. Visa sponsorship is not available for this appointment. 

Pre-employment checks

Your employment is conditional upon the completion of all role required pre-employment or background checks in terms satisfactory to the University. Similarly, your ongoing employment is conditional upon the satisfactory maintenance of all relevant clearances and background check requirements. If you do not meet these conditions, the University may take any necessary step, including the termination of your employment.
 

EEO statement 

At the University of Sydney, our shared values are trust, accountability and excellence and we strive to be a place where everyone can thrive. We are committed to creating a University community that thrives through diversity and reflects the wider community that we serve. We deliver on this through our commitment to diversity and inclusion, evidenced by our people and culture programs, as well as key strategies to increase participation and support the careers of Aboriginal and Torres Strait Islander People, women, people living with a disability, people from culturally and linguistically diverse backgrounds, and those who identify as LGBTIQ+. We welcome applications from candidates from all backgrounds. 

We are proud to be recognised as an Australian Workplace Equality Index (AWEI) Gold employer. Find out more about our work on diversity and inclusion

How to apply

Applications (including a cover letter outlining relevant experience, 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 Rachel Ann Yazigi, Recruitment Operations by email to [email protected].

© The University of Sydney

The University reserves the right not to proceed with any appointment.

Click to view the Position Description for this role.

Applications Close

Sunday 15 February 2026 11:59 PM

Other facts

Tech stack
Clinical Trial Coordination,Data Capture,Good Clinical Practice,Ethics Guidelines,Communication,Planning,Organization,Attention to Detail,Research Environment

About GDG on Campus | University of Sydney

At GDG USYD, we unite students and tech enthusiasts with the common goal of using technology for good. 💻🪴🌏

To this end, our community orchestrates initiatives designed to empower young professionals to drive solutions that have an impact felt locally and globally. Supported by Google, we provide exclusive access to exceptional resources and a vast network.

Team size: 11-50 employees
LinkedIn: Visit
Industry: Technology, Information and Internet
Founding Year: 2021

What you'll do

  • The Clinical Trial Coordinator will support the end-to-end clinical trial process, ensuring smooth operations from planning to execution. They will also handle data capture and verification while building relationships with research staff and stakeholders.

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Frequently Asked Questions

What does a Clinical Trial Coordinator do at GDG on Campus | University of Sydney?

As a Clinical Trial Coordinator at GDG on Campus | University of Sydney, you will: the Clinical Trial Coordinator will support the end-to-end clinical trial process, ensuring smooth operations from planning to execution. They will also handle data capture and verification while building relationships with research staff and stakeholders..

Why join GDG on Campus | University of Sydney as a Clinical Trial Coordinator?

GDG on Campus | University of Sydney is a leading Technology, Information and Internet company.

Is the Clinical Trial Coordinator position at GDG on Campus | University of Sydney remote?

The Clinical Trial Coordinator position at GDG on Campus | University of Sydney is based in Camperdown, Victoria, Australia. Contact the company through Clera for specific work arrangement details.

How do I apply for the Clinical Trial Coordinator position at GDG on Campus | University of Sydney?

You can apply for the Clinical Trial Coordinator position at GDG on Campus | University of Sydney directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about GDG on Campus | University of Sydney on their website.