Clinical Project Co-ordinator - Site Monitor
- Sydney, NSW
- Temporary
- Full-time
Location: Sydney| Full-Time | PermanentMake a meaningful impact on health outcomes through innovative clinical trials.
Are you passionate about clinical research and ready to contribute to cutting-edge, investigator-led trials? Join a dedicated team at the AGITG within their Clinical Research Centre (CRC) as a Clinical Research Associate (CRA). This is a fantastic opportunity to play a key role in improving healthcare while developing your career in a collaborative and purpose-driven environment.About the Role
As a CRA, you’ll be at the forefront of trial delivery—supporting the full trial lifecycle from setup to close-out across multiple clinical sites. You’ll collaborate with internal team members, site investigators, vendors, and clinical site staff to ensure high-quality, ethical trial conduct aligned with Good Clinical Practice (GCP) and regulatory requirements.
This role involves a mix of on-site and remote monitoring and requires domestic travel.Key Responsibilities
- Conduct site feasibility, start-up, initiation, monitoring, and close-out visits
- Ensure data quality through source data verification and adherence to protocol
- Support ethics and regulatory submissions, including TGA applications
- Maintain the Trial Master File and essential study documents
- Provide guidance and training to site teams and monitor site performance
- Work collaboratively with study chairs, investigators, and CRC team members
- Contribute to trial planning, documentation, and reporting
- Lead issue resolution and ensure participant safety and compliance
You’re a proactive and detail-oriented clinical research professional with:
- A degree in a relevant discipline (e.g., life sciences, health, clinical research)
- Solid experience in clinical trial monitoring within academia, CRO, or pharma where Oncology experience would be highly desirable
- In-depth knowledge of ICH GCP and Australian regulatory frameworks
- Strong communication skills and a collaborative mindset
- The ability to manage competing priorities while maintaining high accuracy
- A valid Australian driver’s licence and willingness to travel domestically
- Experience in oncology clinical trials
- Strategic thinking and a solutions-focused approach
- Confidence in managing trial documentation and site communications
At AGITG you’ll be part of a supportive, multidisciplinary team committed to advancing health through innovative research. You’ll have the chance to work on high-impact studies and build strong relationships across the research network while contributing to national and international trial success.Ready to make a difference in clinical research?
Apply now and join a team where your work truly matters.APPLY NOWInterested in this job?Save JobShare this JobCreate AlertSimilar JobsConsultant Name: Consultant Email: Social AccountsSCHEMA MARKUP ( This text will only show on the editor. )Welcome to On Q Recruitment, a specialist Sydney based Life Sciences and Government recruitment agency.