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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