The role includes, but is not limited to the following:
- Adhere to protocols, ethical and regulatory requirements and GCP guidelines at all times for assigned trials
- Manage and coordinate participants throughout the study
- Preparation, dispensing and administration of the investigatory product
- Study-related data entry - source, CRF and site file management
- Work with the study team, including ethics, recruitment, coordinators and Investigators
About you:
You must be a team player with excellent communication skills. Having experience using variety of computer applications, databases and electronic medical records. Sharing our values of Respect and Responsibility, Collaboration, Quality and Safety, and Resilience.
Other Essential criteria:
- 2–3 years' experience as a Lead Clinical Trial Coordinator.
- Ability to work independently and as part of a team
- Exceptional organisational skills and attention to detail
- Time management skills with the ability to manage a range of clinical research activities, prioritise tasks and meet deadlines
- Flexible and open to change and excellent problem-solving ability
- Nurse AHPRA Registration
- Experience working as a coordinator as blinded/unblinded on commercially sponsored clinical trials
- Knowledge and understanding of, GCP, regulatory, ethics, privacy and other applicable guidelines
- Sample preparation and shipping experience
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