Conducts clinical trial procedures in compliance with study protocols, GCP, SOPs, and applicable regulatory requirements
Monitors participant safety and well-being, identifies and manages Adverse Events (AEs/SAEs), and ensures timely documentation and reporting
Administers study and concomitant medications per protocol with accurate and complete documentation
Supports the Principal Investigator by communicating directives, assisting with laboratory data review, and providing study status updates
Maintains accurate, compliant clinical documentation, including participant charts, AEs, and concomitant medications
Provides administrative and operational support to ensure successful conduct of clinical study activities
Education:
Nursing degree required with current in-state licensure
Experience:
1–2 years of experience in a clinical research environment preferred
Equivalent combination of education and experience may be considered
Certification/Licensure:
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