Senior Clinical Research Associate

September 20

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Alimentiv

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

Description

• Manage full clinical site monitoring services for projects. • Act as subject matter expert and mentor for CRAs. • Identify and recruit site investigators and support trial processes. • Primary contact for investigational site queries and overall study integrity.

Requirements

• The successful candidate will possess a minimum of a college diploma/degree and 4-6 years of related experience. • The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results. • Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results. • 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

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