Clinical Research Associate

Role overview

Avania is recruiting an experienced Clinical Research Associate (CRA) / Field Clinical Specialist (FCS) to be based in Sydney. In this position, you will oversee multiple studies running at the same time and support the full clinical trial lifecycle, from regulatory submissions through to site close-out. The role spans site operations as well as sponsor-facing coordination.

Key duties

• Take ownership of study start-up and initiation activities for clinical investigations, including ethics committee and national competent authority submissions, site monitoring preparation, on-site monitoring, and close-out work.
• Serve as the study lead for several simultaneous studies.
• Act as the primary contact person for sponsors.
• Independently manage smaller clinical investigations.
• Support larger clinical investigations by coordinating with other CRAs, contractors, and the Project Manager.
• Train study sites on how to carry out clinical investigations.
• Spot issues and risks that may delay project delivery and work with the Project Manager to put corrective actions in place.
• Resolve site-level findings promptly after monitoring visits.
• Arrange and actively contribute to sponsor, investigator, and project meetings.
• Share regular progress reports and updates with team members and management, while keeping the Project Manager informed.
• Assist the Project Manager in project execution and coordination.
• Contribute to task forces and, where assigned, take on specialist responsibilities such as Subject Matter Expert duties.

Work environment

The role sits within a varied and international environment covering first-in-human pivotal studies, post-market studies, and work across medical devices, IVDs, biologics, and device-drug combination products. Avania operates with a tailored approach across a broad client base, including startups and multinational organizations.

Requirements

• Master’s degree in life sciences, a scientific or nursing discipline, or equivalent training and experience.
• At least 3 years of relevant experience working as a Clinical Research Associate.
• Must be based in Sydney and work from the Sydney office when not travelling.
• Strong attention to detail.
• Comfortable working in a team-oriented environment.
• Excellent communication skills, including the ability to train others.
• Working knowledge of ISO 14155 and/or ICH-GCP E6.
• Ability to travel domestically.
• Good computer and software system proficiency.

Benefits

• Chance to contribute to innovative, cutting-edge medical device clinical trials.
• Ongoing learning and regular training opportunities.
• Supportive, collaborative, and experienced team culture.
• Competitive compensation and benefits package, with details discussed during interviews.
• Opportunity to build a career path without being treated as just a number.
• Team events and full-team meetings.
• Part of a growing global company while working in the APAC region.
• Fast-tracked promotion opportunities for strong performance and engagement.
• Access to scientific medical device leadership and global operational expertise.
• Annual in-house training activities that promote knowledge sharing, open communication, and camaraderie.
• Flexible work options across Australia and New Zealand, with offices in Melbourne and Sydney.

About Avania

Avania provides a complete range of clinical trial services across the Asia Pacific region as part of a global organization. The company values teamwork and collaboration, and supports professional development in a diverse, supportive environment.