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Research Study Assistant (Sleep Research)

Proclinical Staffing
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GENERAL SUMMARY: 

  • Under limited supervision, carries out research projects within guides of regulatory compliance and/or Code of Federal Regulation. 
  • Duties include but are not limited to interacting with both internal and external customers at all levels and completing day to day operational tasks for the study. 
  • Direct contact with potential and enrolled study participants expected. 
  • Analyzes protocol specific requirements and implements measures to ensure stakeholder compliance. 
  • May coordinate low-moderate complexity research projects. 
  • Provides other support as required. 

EDUCATION/EXPERIENCE REQUIRED: 

  • Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology or related field.
  • 1 year experience working at the assistant level supporting clinical research studies 
  • Pharmaceutical clinical trials is a plus.