Clinical Research Associate I - II

September 16

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

201 - 500

Description

• Support and observe clinical site monitoring services • Conduct remote data review and support management activities • Coordinate delivery of clinical site communications • Successfully complete CRA development track activities • Identify and recruit site investigators and optimize patient recruitment

Requirements

• A minimum of a college diploma/degree • 1-3 years related experience • SoCRA, CCRA and/or ACRP certification/designation is an asset • Self-motivation with strong communication skills • Commitment to achieving positive results • Strong attention to detail • Understanding of building collaborative relationships to achieve results

Benefits

Home-based Regular travel