Senior Clinical Research Associate

September 20

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Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management

201 - 500

Description

• Manage clinical site monitoring services for complex, multinational projects • Act as subject matter expert, mentor, and coach CRAs • Lead CRA role may include managing monitoring services for projects • Oversee site recruitment and setup and ensure patient recruitment • Facilitate communication and compliance with project and regulatory guidelines

Requirements

• Minimum of a college diploma/degree and 4-6 years of related experience • Self-motivation with strong communication skills and a commitment to achieving positive results • Strong attention to detail with importance on building collaborative relationships • Ability to engage in continuous learning and self-development • Ability to continually foster teamwork • Fluent in the reading, writing and speaking of English

Benefits

• Home-based • Regular travel