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Clinical Trials Coordinator
2 weeks ago
About Royal North Shore Hospital and the Department of Renal Medicine
Royal North Shore Hospital, a principal tertiary referral hospital for Northern Sydney Local Health District, offers complex medical services to patients across Northern Sydney. With a proud history in education, research, and clinical care, the hospital provides specialty services including major trauma, severe burns, spinal cord injuries, neonatal intensive care, bone marrow transplantation, and neurosurgery among others. It also offers acute medical, surgical, mental health, paediatric, cancer, and maternity services.
Royal North Shore Hospital
was ranked as the third best hospital in Australia, based on the Newsweek
2023 World's Best Hospitals
list.
The Department of Renal Medicine at Royal North Shore Hospital is an internationally recognised leader in pioneering research and clinical excellence in kidney disease. We have conceived, led and executed landmark clinical trials that have set the standard for kidney care worldwide, including the CREDENCE trial, which transformed treatment for patients with diabetic kidney disease; the TESTING trial, which showed that steroids reduce the risk of kidney failure in IgA nephropathy; and the IDEAL trial, a foundational study in dialysis initiation strategies.
Role Description
This is a full-time role for a Clinical Trials Coordinator located at Royal North Shore Hospital, with a hybrid work arrangement allowing some work from home. The Clinical Trials Coordinator will oversee the day-to-day management of clinical trials, including patient recruitment, scheduling, and follow-up. They will ensure compliance with regulatory requirements, manage trial documentation, liaise with stakeholders, and monitor trial progress. Additionally, the Coordinator will assist with data collection and analysis, reporting, and maintaining high standards of patient care and data integrity.
Qualifications
- Experience in Clinical Trials Coordination and management
- Knowledge of regulatory requirements and Good Clinical Practice (GCP)
- Skills in Patient recruitment, scheduling, and follow-up
- Experience in managing trial documentation and liaising with stakeholders
- Proficiency in data collection, analysis, and reporting
- Excellent organizational and communication skills
- Ability to work independently and as part of a team
- Bachelor's degree in Medicine, Nursing, Clinical Research, or related field
- Experience in a hospital or clinical setting is a plus
