· 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 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 significant 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 Current Zealand (Open to Visa Transfer Sponsorship in AUS)
· This prospect is being advertised by Syneos Health Australia Pty Ltd. Be careful
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📌 Cra Ii: Site Monitoring Melbourne
🏢 Syneos Health
📍 Melbourne