Job Summary
A company is looking for a Site Administrator to support the daily operations of clinical trials.
Key Responsibilities
- Assist with the coordination and execution of clinical research studies in compliance with protocols and regulations
- Screen and recruit study participants and maintain accurate study documentation
- Prepare study materials and support the research team in compiling reports and preparing data for analysis
Required Qualifications
- High school degree or equivalent
- At least 1 year of experience in a clinical research setting
- Proficiency in clinical research and general medical terminology
- Current GCP certification and other relevant certifications may be obtained during orientation
- Valid category B driver's license
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