Clinical Research Coordinator – Penrith (NEW Site)
Full-Time | Site-Based
Join a growing, multi-site clinical trials network and play a key role in delivering high-quality research across a diverse range of therapeutic areas. This is an excellent opportunity for an experienced Clinical Research Coordinator to contribute to a newly established site in Penrith.
About the Role Reporting to the Site Director, you will coordinate and manage clinical trials from start-up through to close-out, ensuring compliance with protocols, ICH-GCP, and regulatory requirements.
Key responsibilities:- Coordinate study activities, visits, and timelines
- Manage participant engagement, recruitment, and follow-up
- Maintain accurate source data, EDC/CTMS entries, and essential documents
- Ensure compliance with GCP, TGA, and ethics requirements
- Report AEs/SAEs and manage protocol deviations
- Support monitoring visits, audits, and study close-out
- Liaise with Sponsors, CROs, Investigators, and internal teams
About You- Experience coordinating pharmaceutical-sponsored clinical trials
- Background in Nursing, Allied Health, or Life Sciences (Nursing preferred)
- Strong knowledge of ICH-GCP and clinical trial processes
- Proficient with CTMS and EDC systems
- Highly organised with excellent attention to detail
- Strong communication skills and a collaborative approach
- Ability to manage multiple studies and work independently
Why Join?- Be part of a new site launch in Penrith
- Work across Phase I–IV trials in diverse therapeutic areas (vaccines, respiratory, cardiometabolic, dermatology, and more)
- Supportive, collaborative team environment
- Opportunity to grow within a leading clinical trials network
Take the next step in your clinical research career and help shape a high-performing site from the ground up.
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