Clinical Trial Coordinator and Monitor
About the job
This job is about coordinating and monitoring high-impact infectious diseases clinical trials across Australia within an international research network. It plays a crucial role in advancing global infectious diseases practice and policy, contributing to improved patient outcomes. The team values collaboration, continuous learning, and a supportive environment, making it an exciting opportunity for those passionate about making a difference.
You'll be responsible for
📄
Coordinating ethics and regulatory submissions
Coordinate ethics, governance and regulatory submissions, including amendments, annual reports and site-specific documentation across Australian sites.🤝
Supporting clinical sites
Support clinical sites as primary contact, managing agreements, payments, communications, and facilitating site initiation and training.📂
Maintaining trial documentation
Maintain high-quality trial documentation, including Trial Master Files, Investigator Site Files, templates and audit-ready study and monitoring records.Key criteria
🎓
Tertiary qualification in health sciences
Possession of a relevant degree in Life or Health Sciences.View
📊
Clinical research coordination experience
Demonstrated experience in coordinating or monitoring clinical trials.View
📜
Knowledge of Good Clinical Practice
Understanding of GCP and Australian regulatory frameworks.View
View more
