Clinical Research Associate, Full Service

Lifelancer
Durham, NC
Category Research
Job Description
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • Completion of CRA training program or prior monitoring experience
  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements
  • Good therapeutic and protocol knowledge
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
  • Written and verbal communication skills

Benefits

  • IQVIA is proud to be an equal opportunity employer
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