Clinical Research Assistant- Hybrid

• Assist PI in development of protocol-specific tools to aid in study documentation
• Assess eligibility of research subjects in accordance with the approved protocol and all applicable regulations including HIPAA
• Obtain patient consent and Human Subject Committee approvals for minimal-risk studies as delegated by IRB-approved protocol
• Collect, record, evaluate, update, and store/transport pertinent data and samples in relation to protocol
• Track study enrollment and completion of milestones
• Summarize research findings and prepare presentations
• Perform literature searches
• Schedule patient tests and/or interviews
• Conduct patient telephone follow up
• Stock, inventory, store, and order samples/supplies as needed to maintain appropriate operations
• Review medical records and medical record abstractions for consistency and completeness
• Comply with established policies, health and safety regulations and requirements, procedures, and department objectives
• Maintain patient and study subject confidentiality
• Perform other duties as required.
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  Qualifications
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  REQUIRED QUALIFICATIONS:
  • Bachelor's degree in a scientific or health care field, or related experience
  • Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
  • Oral and written communication skills
  • Excellent organizational and interpersonal skills required.PREFERRED EXPERIENCE:
    • Experience recruiting, screening, and interviewing research participants preferred
    • REDCap and SPSS knowledge and skills preferred
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      

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