Found Description
Overview
- Coordinate and manage clinical monitoring activities across all trial phases and therapeutic areas
- Full service CRO with in-house regulatory affairs consultancy
- Sydney-based role with multiple positions available across NSW
Benefits
- Work for a leading CRO across Asia-Pacific
- Regular training and international knowledge-sharing opportunities
- Get exposure to a diverse range of therapeutic areas
About the company
Our client is a respected global CRO with an established presence across multiple regions, providing end-to-end clinical development services to pharmaceutical, biotechnology and medical device organisations.
About the opportunity
Acting as the primary link between the sites and the sponsor, the CRA will coordinate and manage clinical monitoring activities from site start-up through to close out.
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