In-Demand Trial study coordinator Jobs in New South Wales

Clinical Trial Coordinator
KG Talent —Sydney NSW
- Full-time
- Research
- Microsoft Office
- Computer skills
Quick Apply
Clinical Trial Coordinator II
Thermo Fisher Scientific —Sydney NSW
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Parental leave
- Employee assistance program
Clinical Research Cordinator
GenesisCare —Lake Macquarie NSW
- Part-time
- Vital signs
- Patient monitoring
Clinical Research Centre Research Assistant
The Sydney Children's Hospitals Network —Sydney NSW
- $78,183.85 - $79,973.57 a year
- Full-time
- Research
- Microsoft Office
- Recruiting
- Employee assistance program
8d
Clinical Project Manager (Oncology)
Tardis Group —Sydney NSW
- Management
- Research
- Presentation skills
Provisional Fellow
NSW Health —Concord NSW
- $117,745 - $147,664 a year
- Call employer
- Research
- Patient care
- Communication skills
Senior Resident Medical Officer
Western Sydney Local Health District —Sydney NSW
- $94,521 - $127,827 a year
- Part-time
- Medicine
- Research
- Communication skills
Senior Resident Medical Officer
NSW Health —Westmead NSW
- $94,521 - $127,827 a year
- Part-time
- Medicine
- Research
- Communication skills
Nurse Educator
St Vincent's Health Australia —Inner West NSW
- $135,826.04 - $138,534.10 a year
- Full-time
- Clinic
- Communication skills
- Teaching
6d

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Clinical Trial Coordinator

KG Talent
Sydney NSW

Quick Apply

Job Details

Full-time

Qualifications

Research
Microsoft Office
Clinical trials
Computer skills
Communication skills
Time management

Full Job Description

Clinical Trial Coordinator | Key Health Medical Centre

Help Advance Medical Research That Makes a Difference

Key Health Medical Centre is seeking a highly organised and motivated Clinical Trial Coordinator to join our growing Clinical Research Unit (CRU) based in Sydney CBD South.

This is an exciting opportunity to work alongside experienced Research Nurses, Principal Investigators, and sponsors to help deliver high-quality clinical trials that contribute to improving patient care and advancing medical research.

If you're detail-oriented, enjoy working in a fast-paced healthcare environment, and are passionate about research and clinical excellence, we'd love to hear from you.

About the Role

Reporting to the Clinical Trial Manager, you'll coordinate the day-to-day delivery of multiple clinical trials, ensuring each study is conducted safely, ethically, and in accordance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.

You'll work closely with Research Nurses, Investigator GPs, sponsors, and Contract Research Organisations (CROs), playing a key role in participant coordination, study administration, regulatory compliance, and site operations.

Key Responsibilities

Study Coordination

Coordinate day-to-day activities across multiple clinical trials
Support study start-up activities, including site initiation and essential documentation
Schedule participant visits and coordinate investigator and research nurse availability
Maintain accurate and audit-ready Trial Master Files (TMF/eTMF) and study documentation
Assist with monitoring visits, audits, and regulatory inspections

Participant Coordination

Support participant recruitment, screening, and enrolment activities
Coordinate participant appointments within protocol timeframes
Track participant progress, eligibility, and retention throughout each study

Regulatory & Compliance

Assist with ethics submissions, amendments, continuing reviews, and safety reporting
Maintain regulatory files, delegation logs, and staff training records
Enter and maintain accurate study data within Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS)
Ensure studies comply with ICH-GCP, TGA, HREC, and sponsor requirements

Stakeholder Engagement

Liaise with sponsors, Clinical Research Associates (CRAs), and CRO representatives
Work collaboratively with Research Nurses, GPs, and the Clinical Trial Manager
Assist with study administration, invoicing, ordering study supplies, and maintaining accountability logs

About You

You'll be a highly organised professional who enjoys coordinating multiple priorities while maintaining exceptional attention to detail.

To be successful, you'll have:

A degree in Health Science, Life Science, Nursing, or a related discipline
Previous experience as a Clinical Trial Coordinator, Clinical Trial Administrator, Research Nurse, or similar role is highly regarded
Sound understanding of, or willingness to learn, ICH-GCP and clinical trial regulations
Excellent organisational and time management skills
Strong attention to detail and documentation accuracy
Excellent communication and interpersonal skills
Confidence working with participants, clinicians, sponsors, and research partners
Strong computer skills, including Microsoft Office and the ability to learn CTMS, EDC, and eTMF systems
Current GCP Certification will be highly regarded

Why Join Key Health?

Be part of a growing Clinical Research Unit delivering meaningful medical research
Work alongside experienced clinicians and research professionals
Gain exposure to a diverse range of clinical trials
Supportive and collaborative team culture
Modern CBD South location
Opportunities for ongoing learning and professional development

If you're looking to build your career in clinical research and want to contribute to studies that improve patient outcomes, we'd love to hear from you.

Apply now and join the Clinical Research Unit at Key Health Medical Centre.

Quick Apply

Refine Your Search

trial study coordinator jobs in new south wales

Clinical Trial Coordinator

Clinical Trial Coordinator II

Clinical Research Cordinator

Clinical Research Centre Research Assistant

Clinical Project Manager (Oncology)

Provisional Fellow

Senior Resident Medical Officer

Senior Resident Medical Officer

Nurse Educator

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