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Study Coordinator

Study Coordinator

  • Coordinate client studies based on study protocols and according to regulatory guidelines
  • Ability to conduct a broad range of study procedures without supervision and the ability to troubleshoot experimental problems when necessary
  • Pre-clinical experience 
  • Perform various animal dosing techniques such as oral and IV administration
  • Perform and/or oversee various biological sample collection procedures such as blood, urine, fecal, and tissue samples
  • Continually work to adapt and improve systems (experimental data collection) to make them more efficient and effective
  • Draft and write SOPs and procedures
  • Draft deviation and protocol amendments
  • QC study protocols and/or reports
  • Prepare raw data notebooks and pertinent records, and ensure these records are in compliance with applicable federal guidelines
  • Participate in training and oversight of study technicians and aid utilization of their time effectively

Requirements:

  • Minimum of a BA 
  • 2 years of pre-clinical experience
  • High degree of technical proficiency to serve as a trainer to technicians in multiple areas
  • High level of attention to detail and familiarity with variety of study types
  • Ability to work efficiently under tight time constraints and as a member of a team
  • Strong written work      

 

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