Clinical Research Associate

November 27

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501 - 1000 employees

Founded 1961

Description

• The CRA executes clinical monitoring activities at clinical trial sites • Supports start-up and provides local expertise • Collaborates closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to

Requirements

• Ideally 2-4 years of (CRA) monitoring experience in the pharmaceutical or CRO industry • Excellent communication and interpersonal skills • Excellent organizational skills and ability to prioritize and multi-task • Fluent in English and French (writing and speaking)