We are seeking exceptional Senior Clinical Research Associates (CRAs) to join our growing Clinical Operations team in Australia.
You will monitor sites across Australia and have the flexibility to work from home.
You will also be employed permanently by Covance.
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 have a role for you.
Your responsibilities will include:
- Leading all aspects of study site monitoring according to company SOPs, 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.
Covance Australia is committed to providing Clinical Research Associates; flexibility to work from home, the freedom to grow your career across all phases and areas of clinical trial operations, and provides you with cutting edge technology and processes that help to manage your time and workload.
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