Clinical Trials Coordinator (Health Mgr Lvl 1) - Temp PT

NSW Health; Liverpool; Vor Ort; AUD 63.000 - 84.000; Teilzeit

Benefits dieser Stelle

Annual leave 17.5% loading

Hybrid work options

Parental leave

Zusammenfassung

NSW Health in Liverpool is seeking a Clinical Trials Coordinator to support a portfolio of investigator-initiated and industry-sponsored trials in a busy Interventional Radiology department. You will coordinate trials from start-up through close-out, facilitate new devices and treatment approaches, and help provide patients access to cutting-edge healthcare.

The role requires strong organizational skills, ICH-GCP knowledge, and the ability to manage documentation and study data with a

Qualifikationen

• Proven experience coordinating clinical trials in healthcare or research.
• Sound knowledge of ICH-GCP and ethical/regulatory requirements.
• Experience preparing Ethics and Governance submissions.

Aufgaben

• Coordinate trials from start-up to close-out.
• Support study budget negotiations and device introductions.
• Engage with sponsors, clinicians, nurses and researchers to ensure compliance.

Kenntnisse

Interpersonal skills

Communication

Stakeholder engagement

Regulatory understanding

Ausbildung

Tertiary qualifications in a relevant discipline

Tools

MS Word

Excel

eCRF databases

Jobbeschreibung

Clinical Trials Coordinator (Health Mgr Lvl 1) - Temp PT

South Western Sydney Local Health District

REQ698818

Requisition ID: REQ698818
Employment Type: Temporary Part time, 16 hours per week until 15/10/2027
Remuneration: $46.05 - $61.27 per hours+ 12% Superannuation + Salary Packaging
Location: Liverpool Hospital
Applications close: 18/10/2026
Contact: Anson Vo - Clinical Trials Operations Manager on [e-mail]

With your skills and experience, you can contribute to the millions of ways we're enriching health, and develop your career as part of the largest health organisation in Australia.

Achieve Something Great

Join Liverpool Hospital’s Interventional Radiology department and play a key role in delivering innovative clinical research that helps shape the future of patient care. As a Clinical Trials Coordinator, you will support a diverse portfolio of investigator-initiated and industry-sponsored trials, working alongside interventional radiologists, nurses, radiographers and research professionals within a leading tertiary referral and teaching hospital.

This is an exciting opportunity to coordinate clinical trials from study start-up through to close-out, contribute to the introduction of new devices and treatment approaches, and help provide patients with access to cutting-edge healthcare advancements.

Are You the Right Fit?

The ideal candidate will be an organised and detail-oriented research professional with demonstrated experience coordinating clinical trials in a healthcare or research environment. Success in this role requires sound knowledge of ICH-GCP, ethical and regulatory requirements, experience preparing Ethics and Governance submissions, conducting feasibility assessments, supporting study budget negotiations, and implementing clinical trials from study start-up through to close-out, including participant recruitment and management.

Strong communication and stakeholder engagement skills are essential, with the ability to work collaboratively with sponsors, clinicians, nurses, pharmacists, scientists and other health professionals. Experience managing study documentation, case report forms, clinical specimens, data collection and query resolution, while maintaining compliance with regulatory and local requirements, will be highly regarded. A commitment to continuous learning, mentoring others and contributing to the growth of clinical research within the workplace will be highly valued.

Selection Criteria

To help us assess your suitability for the role, please tell us as much as you can about yourself in response to the questions below.

• Tertiary qualifications in a relevant discipline, or demonstrated minimum 2 years experience in the field of research and/or clinical trials.
• Well developed interpersonal, consultation, facilitation, negotiation, and communication skills with a diverse range of internal and external stakeholders.
• Demonstrated understanding and experience in the ethical requirements for research including the NHMRC National Statement and Good Clinical Practice (GCP).
• Demonstrated knowledge and ability to mentor members of the research team to enhance professional development.
• Computer skills including proficiency in the use of MS Word and Excel, email, and understanding of database utilisation such as electronic Case Report Forms (eCRF).
• Ability to work independently and as part of a multidisciplinary team.
• Excellent organisational skills with demonstrated experience working in a high volume and demanding professional environment with proven capacity to prioritise, multi-task, achieve departmental goals with a customer focused approach.
• Ability to engage with all stakeholders involved with clinical trial management to meet contractual and protocol requirements.

If you'd like more details, we’re here to help.

We are proud to be an equal opportunity employer dedicated to accessibility and a supportive recruitment experience. If you require adjustments or assistance during the application process, please contact [e-mail]

We value the diverse backgrounds, experiences, and perspectives of our workforce and are committed to fostering a respectful and welcoming environment. We strongly encourage applications from Aboriginal and/or Torres Strait Islander peoples, people with disability, neurodivergent individuals, those from Refugee, multicultural and multifaith backgrounds, and members of the LGBTQI+ community.

More Than Just a Job – Why Work With Us?

• Annual leave with 17.5% leave loading (for full-time and part-time staff)
• One extra day off each month for full-time employees
• Work-Life Balance
• Flexible work options, including hybrid and varied hours (depending on the role)
• Paid maternity and parental leave
• Generous leave options like long service and carers leave
• Free and confidential support for staff and their families via our Staff Wellbeing and Support Service (EAP)
• Wellbeing programs that promote mental health, resilience, and balance

South Western Sydney Local Health District is dedicated to fostering a child-safe environment that respects and upholds the rights of children and young people, aligned with NSW Health’s commitment to implementingthe Child Safe Standards. We aim to ensure that children and young people feel safe, supported, and included in their care. All current and prospective staff are expected to prioritise the safety, welfare, and well-being of children and young people, actively working to protect them from harm and abuse.

Temporary Positions

For fixed-term or temporary contracts, there may be opportunities for ongoing permanent employment, subject to policy and organisational requirements.

NSW Health acknowledges the people of the many traditional countries and language groups of New South Wales. It acknowledges the wisdom of Elders past and present, and pays respect to all Aboriginal communities of today.