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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