- 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

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 Recent Zealand (Open to Visa Transfer Sponsorship in AUS)
- This opportunity is being advertised by Syneos Health Australia Pty Ltd.

#J-18808-Ljbffr

📌 Clinical Research Associate II (New South Wales)
🏢 Syneos Health Clinical Solutions
📍 New South Wales