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Clinical Research Associate


The CRA helps to plan, coordinate and manage the day-to-day running of clinical studies for cancer in vitro diagnostics, especially Companion Diagnostic studies to support regulatory applications and scientific marketing activities.

Responsibilities include: identify, evaluate and qualify clinical study sites; assist with site contracting and vendor management; ensure GCP monitoring of study sites; responsibility for study files, guiding projects while conforming to requirements; primary point of contact for study related issues at sites; assist in the supervision of trial related information, coordination of EC/IRB approvals and resolution of issues at study sites.

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek ---- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

 

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