CRA II/SCRA. Global CRO. Office based in Sydney or regionally home based.
Your new company This global CRO is recognized as one of the most successful in the industry with long standing sponsor partnerships, they are in search of a passionate Clinical Research Associate to join their expanding core team in Sydney. The CRA is responsible for all aspects of study monitoring and general on-site monitoring responsibilities. Your new role Working in a large team of CRA's you will be independently monitoring clinical trials in line with ICH-GCP guidelines and company SOP's; you will ensure trial data is accurate, complete and verifiable.
You will manage clinical trials at varying stages; from feasibility, site selection, monitoring through to close out. As a member of the CORE clinical monitoring team you will be working on an array of different interesting studies. What you'll need to succeed To be considered for the role, you will have a Bachelor's level degree in life sciences, pharmacy, nursing or another related subject with proven experience in independent multi-site clinical monitoring for eighteen months or more.
You will need to have strong communication, interpersonal and organizational skills as well as demonstrating strong computer skills. What you'll get in return The opportunity to work within a high performing team for a huge global CRO whose clients include the world's biggest pharmaceutical companies. You will be offered excellent training opportunities, dedicated line managers and the opportunity for career progression.
High achievers will be rewarded on a sliding scale of Bronze, Silver and Gold. They will also have the opportunity to work internationally. What you need to do now If you're interested in this role, please forward an up-to-date copy of your CV to ruby.
lewishays.com.au, or call 0281136442.
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