About You

Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed onsite or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance.

Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans.

Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.

Awesome line management supporting team with a huge focus on you!

Value your expertise, listen to your voice and most important work as a team





Forward thinking & innovative CRO which stands out in the industry

Bachelor's degree or College/University degree in Life Sciences or equivalent qualifications

Minimum of 2-years of independent clinical monitoring experience

Excellent communication and interpersonal skills with internal and external stakeholders

Good time management skills and demonstrate critical thinking

Full working rights in Australia or New Zealand (Open to Visa Transfer Sponsorship in AUS)

This prospect is being advertised by Syneos Health Australia Pty Ltd.

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📌 Clinical Research Associate II (Sydney)
🏢 Syneos Health
📍 Sydney