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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.
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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.
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LICENSES AND/OR CERTIFICATIONS
- 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
- 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.
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WORKING CONDITIONS
- Normal office environment with little exposure to excessive noise, dust, temperature and the like.
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PHYSICAL REQUIREMENTS
- Click here to view physical requirements.
Listed under Science & Research jobs.