Senior Clinical Trial Coordinator | Key Health

Help Advance Medical Research That Makes a Difference

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

This is an exciting opportunity for an experienced clinical research professional to take a senior role in the coordination and delivery of high-quality clinical trials.

Working alongside experienced Research Nurses, Principal Investigators, Investigator GPs, sponsors and Contract Research Organisations (CROs), you’ll play an important role in ensuring studies are delivered safely, efficiently and in accordance with protocol, Good Clinical Practice (GCP) and regulatory requirements.

If you have strong clinical research experience, excellent attention to detail and enjoy taking ownership of multiple studies, we’d love to hear from you.

About the Role

Reporting to the Clinical Trial Manager, you’ll take responsibility for the day-to-day coordination and delivery of multiple clinical trials across the Clinical Research Unit.

You’ll work closely with Principal Investigators, Research Nurses, sponsors and CROs, supporting studies from start-up through to close-out.

As a senior member of the team, you’ll also provide guidance and support to other members of the clinical research team and help maintain high standards across study delivery, documentation and compliance.

Key Responsibilities

Study Coordination

- Coordinate and take ownership of day-to-day activities across multiple clinical trials
- Support and lead study start-up activities, including site initiation,



feasibility activities and essential documentation
- Coordinate study timelines, milestones and site activities to ensure protocols are delivered within required timeframes
- Schedule participant visits and coordinate investigator and research nurse availability
- Maintain accurate, complete and audit-ready Trial Master Files (TMF/eTMF) and study documentation
- Support monitoring visits, audits and regulatory inspections
- Identify, manage and elevate study issues, risks and protocol deviations as required
- Support study close-out activities and ensure all documentation is completed appropriately
- Participant Coordination
- Support and coordinate participant recruitment, screening, enrolment and retention activities
- Coordinate participant appointments in accordance with study protocols and required timeframes
- Monitor participant progress, eligibility and retention throughout each study
- Work closely with Research Nurses and investigators to ensure a positive participant experience
- Ensure participant information and study documentation is maintained accurately and securely

Regulatory & Compliance

- Coordinate and support ethics submissions, amendments, continuing reviews and safety reporting
- Maintain regulatory files, delegation logs, training records and other essential documents
- Ensure study documentation is complete,



accurate and inspection-ready
- Enter and maintain accurate study data within Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS)
- Ensure studies are conducted in accordance with ICH-GCP, TGA, HREC and sponsor requirements
- Identify compliance issues and work with the Clinical Trial Manager and investigators to address them

Sponsor & Stakeholder Management

- Build strong working relationships with sponsors, CROs, Clinical Research Associates (CRAs) and study teams
- Act as a key point of contact for day-to-day study coordination and site queries
- Respond to data queries and study requests within required timeframes
- Work closely with Principal Investigators, GPs, Research Nurses and the Clinical Trial Manager
- Support study meetings and provide updates on recruitment, timelines, issues and study progress
- Assist with study administration, invoicing, ordering study supplies and maintaining accountability logs
- Provide guidance and support to Clinical Trial Coordinators, Research Nurses and other members of the research team where required
- Share knowledge and support consistent clinical research processes across the CRU
Assist with onboarding and training new team members
- Contribute to improving systems, processes and documentation within the Clinical Research Unit

About You

You’ll be an experienced clinical research skilled who is confident coordinating multiple studies and working with a range of internal and external stakeholders.

You’ll have solid attention to detail, excellent organisational skills and the ability to take ownership o

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