Clinical research is a critical component of advancing medical knowledge and improving patient outcomes. As a Clinical Research Coordinator, you will play a vital role in the success of our research endeavors.
Key responsibilities include coordinating and conducting study assessments, collecting data as per protocol, working closely with investigators to ensure effective research activities, organizing and maintaining regulatory documentation and study files, screening subjects for eligibility, and ensuring timely completion of study-related documentation and close-out activities.
To excel in this position, you will possess:
* A background in nursing and current AHPRA registration
* Previous clinical trials experience is highly desirable
* Strong patient management and clinical skills (venepuncture, cannulation, infusion)
* A cardiology background is highly valued
* Excellent communication and interpersonal skills, with the ability to work well independently and as part of a team