Clinical Research II

Why The Role Is For 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

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.