Avania are hiring – Clinical Trial Associate (CTA) 

The Clinical Trial Associate (CTA) primarily provides operational support to Clinical Research Associates (CRA), Lead CRAs (LCRA) and Project Managers (PM) and coordinates specified clinical trial activities, but also provides assistance to Clinical personnel as required.

The Clinical Trial Associate’s (CTA) main responsibilities are to maintain the trial master files, ensure the quality and track the status of study documents, oversee study-specific trainings for team members, capture study-specific meeting minutes, produce study-specific binders, possibly interface with Sponsor representatives, suppliers, and site staff.

Additional responsibilities for the role of Clinical Trial Associate (CTA) will include supporting our Sydney office with administrative support, as such will be required to be office based.

When You Need to Advance Your Career, It Takes Avania

Avania is a leading, global full-service contract research organization (CRO) focused on the management of clinical studies for medical devices. Avania supports medical devices, in vitro diagnostics, biologics, and device-drug combination products from innovation to commercialization with a customized approach.

Avania comprises highly specialized regional team members working together on a global scale to improve the future of human health. We work across a wide variety of clinical trials, but specialize in medical devices, innovative technology, and combination products in numerous therapeutic areas.

Because we believe that collaboration yields the best results, you will get to work with experts across many specialties. Avania encourages cross-training and the exchange of knowledge and ideas to help employees grow and advance.