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Job Summary: We are seeking an exceptional Clinical Research Associate to join our extraordinary people in our clinical operations team that monitors Phase I - IV clinical trials.

Job Details:

• Lead all aspects of study site monitoring according to Covance/Chiltern SOP, GCP, and ICH guidelines


• Partner with investigators and study coordinators on pre-study qualification and site initiation visits


• Conduct routine study site monitoring visits


• Close-out clinical sites, and ensure study files are up to date to maintain the success of the study

If you are passionate about Clinical Research and a person who has experience independently monitoring Phase I - IV clinical study sites in Australia, let’s talk as we may have a job for you.