Role: Clinical Site Manager (full- or part-time)
Location: Sydney (home- based), or Melbourne (home-based)
As a Clinical Site Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
In your new role, you will have combined responsibilities of a Senior Clinical Research Associate and of a Site Engagement Liaison. You will be embedeed with one of the world’s leading Biopharmaceutical companies, focused on creating valuable solutions that make improvements to the lives of people living with neurological and autoimmune conditions now and into the future.

WHY ICON?

At ICON, we embrace new perspectives and empower our people to write their own paths forward. We are a culturally diverse company with over 40,000 talented and ambitious people with varied skills, perspectives & backgrounds working together across 40 countries.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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• Maximize site performance and site engagement, leveragging strong clinical operational and therapeutic expertise to support execution of clinical studies
• Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock
• Support CPM in management of the study, including vendor management
• You will be fully embedded in our client’s study team and have a dedicated ICON line manager to support you
• Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and to ensure audit and inspection readyness in collaboratiion with CPM