**Clinical Trial Coordinator Role Summary**
We are seeking an experienced Clinical Research Associate to join our team in Melbourne. As a Clinical Trial Coordinator, you will be responsible for planning and executing clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.
Main Responsibilities:
* Plan and execute clinical trials, ensuring compliance with relevant standards.
* Work closely with investigators, study teams, sponsors, and healthcare staff to ensure smooth trial operations.
* Prepare and submit applications to ethics committees and governance bodies.
* Manage recruitment, informed consent processes, scheduling, and monitoring of participants' progress.
* Maintain accurate trial records and prepare reports for stakeholders.
* Monitor timelines, budgets, milestones, and project deliverables effectively.
Requirements:
* Nursing background or Scientific Background
* Good Clinical Practice (GCP) certification is highly desirable.
* Experience coordinating clinical trials across various phases.
What We Offer:
* A competitive salary.
* Professional development opportunities.
* The chance to work on cutting-edge research that has a real impact on patient outcomes.