Oversee all stages of clinical trials across a wide scope of therapeutic areas
Full service CRO
Remote / on-site hybrid role
Work for a global leading CRO
Work on an inclusive team that encourages career growth
Get exposure to a diverse range of therapeutic areas
Attractive salary package
About the company
Our client is a fast-growing CRO company. You will work across multiple therapeutic areas across all phases. Join a close kit team that emphasises support and valuing employee contribution.
About the opportunity
The CRA/SCRA will act as the primary link between the sites and the sponsor and will oversee all stages of trials from initiation through to close out.
Prepare, organise, conduct and follow-up routine monitoring and close out visits as per relevant study plan
Motivate and train investigators and site staff to ensure obligations in regard to study timelines
Ensure compliance with ICH/GCP, study protocols and other applicable regulatory guidelines
Oversee all ethics submissions and trial reporting
Follow company SOP’s and adapt knowledge and processes as applicable to the therapeutic area
Contribute to process improvements and protocol review
Tertiary degree in life sciences or relevant subject
At least 12 months independent monitoring experience
Ideally experience working in a research institution or CRO
In depth knowledge of ICH / GCP guidelines
Highly organized with excellent communication skills
Full Australian working rights
Highly dynamic CRO that is expanding its presence in the APAC region. Join a fast growing and innovative company that awards hard work.
How to Apply Click apply or contact one of our consultants for a confidential discussion: Davina Ocansey, Senior Recruitment Consultant on +61 2 8877 8712 Mattias Fitzgerald, Recruitment Consultant on +61 2 8877 8749
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