Senior Clinical Research Coordinator - Full Time
The Role:
The role is Full Time and is in office.
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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