Location: Warsaw, Indiana (MUST work on-site)

Duration: 1-year (possibility of extension)

Pay: $56,784 plus benefits


Under the direction of the Principle Investigator, the Clinical Research Coordinator is responsible for executing study procedures as prescribed by the clinical protocol, ensuring the quality and integrity of data.


  • Manage investigation site activities
  • Discuss and effectively resolve issues associated to site
  • Maintain clinical trial supplies, track patient recruitment activities, manage regulatory documentation
  • Complete Case Report Forms accurately and complete query resolution
  • Attend procedures and collect study protocol data collection
  • Participate as needed in Investigator meetings
  • Maintain Investigator Site Fil


  • Bachelors degree
  • 1-3 years of Clinical Research related experience
  • Knowledge of FDA guidelines, regulations and Good Clinical Practice
  • Highly developed communication and organizational skills
  • Computer skills required (Microsoft Office products Word, Excel, PowerPoint, Project and SharePoint)

Required Qualifications

  • None

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