Job Description
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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.
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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.
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Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.
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Awesome line management supporting team with a huge focus on you!
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Value your expertise, listen to your voice and most significant work as a team
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Forward thinking & innovative CRO which stands out in the industry
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About You
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Bachelor's degree or College/University degree in Life Sciences or equivalent qualifications
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Minimum of 2-years of independent clinical monitoring experience
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Excellent communication and interpersonal skills with internal and external stakeholders
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Good time management skills and demonstrate critical thinking
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Full working rights in Australia or New Zealand (Open to Visa Transfer Sponsorship in AUS)
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This opportunity is being advertised by Syneos Health Australia Pty Ltd.
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📌 Clinical Research Associate Ii (New South Wales)
🏢 Syneos Health Clinical Solutions
📍 New South Wales