Research Assistant (Non-Clinical)
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Summary
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GENERAL SUMMARY
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The Research Assistant participates as a member of the Clinical Research Unit and is responsible for supporting clinical research studies. Requires strong attention to detail and excellent organizational skills. Reports to department leadership.
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ESSENTIAL DUTIES AND RESPONSIBILITIES
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Manages trial supplies; acts as point of contact for monitors, vendors and sponsors related to receipt, use, and return of supplies.
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Processes, packages and ships laboratory specimens.
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Coordinates trial system access, equipment and deliveries with vendors.
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Assists with onsite and remote study monitoring visits by sponsors.
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Prepares materials for subject visits.
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Assists with data management.
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Performs other duties as assigned.
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LICENSES AND/OR CERTIFICATIONS
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IRB (Institutional Review Board) certification in human subject’s protection required, or must be completed within 90 days of hire.
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MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS
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Associate’s degree in Human Services or closely related field preferred.
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Previous experience in laboratory and research preferred.
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Demonstrated ability to analyze and problem solve independently.
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IATA (hazardous materials training) required.
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Knowledge of procedures governing clinical research preferred.
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WORKING CONDITIONS
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Normal office environment with little exposure to excessive noise, dust, temperature and the like.
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PHYSICAL REQUIREMENTS
