Job Description

• GENERAL SUMMARY

• 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.

• ESSENTIAL DUTIES AND RESPONSIBILITIES

• Manages trial supplies; acts as point of contact for monitors, vendors and sponsors related to receipt, use, and return of supplies.

• Processes, packages and ships laboratory specimens.

• Coordinates trial system access, equipment and deliveries with vendors.

• Assists with onsite and remote study monitoring visits by sponsors.

• Prepares materials for subject visits.

• Assists with data management.

• Performs other duties as assigned.

• LICENSES AND/OR CERTIFICATIONS

• IRB (Institutional Review Board) certification in human subject’s protection required, or must be completed within 90 days of hire.

• MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS

• Associate’s degree in Human Services or closely related field preferred.

• Previous experience in laboratory and research preferred.

• Demonstrated ability to analyze and problem solve independently.

• IATA (hazardous materials training) required.

• Knowledge of procedures governing clinical research preferred.

• WORKING CONDITIONS

• Normal office environment with little exposure to excessive noise, dust, temperature and the like.

• PHYSICAL REQUIREMENTS

• Click here to view physical requirements. (

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