Role OverviewAssists the Principal Investigator and study team on delegated duties to support clinical trials, under the direct supervision of senior research staff.
What You Will Do
Assists with organization and maintenance of study files, recruitment and retention of research subjects, study visits and procedures, and processing, storage, and shipment of research samples.
Why It Might Be a Fit
Must have excellent communication and organizational skills, knowledge of medical terminology, and familiarity with basic laboratory equipment.
Requirements
- High School Equivalent / GED
- Certification in Human Subjects Protection (CITI)
- DOT/IATA Training
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