Clinical Trial Administrator (Oncology) – Northern Suburbs Are you passionate about making a real impact in clinical research? Do you have an eye for detail and a talent for organization? Join our dynamic team as a Clinical Trial Administrator (CTA) and help drive the development of innovative oncology treatments. About: As a Clinical Trial Administrator, you’ll play a vital role in the successful execution of clinical trials. You’ll support the clinical research team by coordinating trial documentation, managing key regulatory and logistical processes, and ensuring compliance with Good Clinical Practice (GCP) and applicable regulations. Responsibilities: Maintain and manage the Investigator Site File (ISF) and other essential clinical documents Support study start-up, conduct, and close‑out activities Coordinate investigator and ethics committee submissions Track study progress and timelines Assist with the scheduling of monitoring visits, meetings, and site communications Ensure accuracy and completeness of data in tracking systems Requirements: Previous experience in a similar CTA or clinical operations support role (preferred) Strong organizational skills with high attention to detail Working knowledge of ICH‑GCP and clinical trial processes Excellent written and verbal communication skills Proficient in Microsoft Office and clinical trial management systems (CTMS) Please submit your CV and motivational letter to Kindly include your salary expectation in your application. Closing date for applications: 24 June 2025 #J-18808-Ljbffr