Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed onsite or remotely) ensuring regulatory, ICH-GCP and/or Valuable 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 responsible 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 key work as a team




Forward thinking & innovative CRO which stands out in the industry

About You
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 opportunity is being advertised by Syneos Health Australia Pty Ltd.
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📌 Clinical Research Associate Ii Sydney
🏢 Syneos Health Clinical Solutions
📍 Sydney