Clinical Research Study Coordinator

 JOB8
 Australia, , New South Wales
 1 week, 5 days ago
Cabrini Cabrini is a Catholic charitable organisation inspired by the spirit and vision of Saint Frances Xavier Cabrini and the Missionary Sisters of the Sacred Heart of Jesus. This order was founded by Saint Frances Xavier Cabrini who was canonised in 1946 and later proclaimed Universal Patron Saint of Immigrants. We are a community of care, reaching out with compassion, integrity, courage and respect to all we serve. With more than 4300 staff, 1000 accredited medical practitioners and several locations, we offer a range of employment opportunities to start, continue or advance your career. The Role The Clinical Research Study Co-ordinator provides assistance to the Oncology Clinical Trials Team within the Department of Medical Oncology at Cabrini, contributing to the development of clinical research, and working within the framework of the Mission and Values of Cabrini Health. You will have the opportunity to work within our Oncology Clinical Trials Team and gain valuable hands on experience. You will be a productive member of the team and will be mentored and supported as you develop your skills. This position is full time (1 FTE). Key Capabilities Implements and assists in co-ordination of clinical trials carried out at Cabrini Institute. Provides administrative support including but not limited to data management activities, and Investigator Site File and project tracking tool maintenance from start up to close out of trials. Adheres to clinical trial protocols. Ensures compliance with all regulatory, state, national, and internationally accepted guidelines for Good Clinical Practice in research (ICH GCP). This includes: Ensures protocols and Investigator Drug Brochures are current Awareness of protocol specific issues Ensures patient screening baseline tests are completed according to protocol requirements Informs patients of all relevant aspects of the trial Organises patient schedules as per protocol requirements Liaises with other departments regarding protocol requirements and ensures compliance Reports serious adverse events to all relevant stakeholders promptly Maintains a log of trial participants and identifies barriers to participation and solutions to facilitate participation Adheres to accurate and timely entry of data into paper and/or computer based systems Liaises with monitors of clinical trials and is ready for monitoring and/or auditing as required, with full patient documentation available. Tertiary degree in a science or nursing background preferred. Applicants must possess a valid work visa. Cabrini Offers Attractive rates & benefits Salary Packaging Professional development opportunities Close to public transport Cabrini is an equal opportunity employer Cabrini is committed to providing a safe environment for children Compassion - Integrity - Courage - Respect

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