Project Coordinator- Lyon, France

Responsibilities

  • Daily engagement with clinical trial management;
  • Compile and maintain project-specific status reports;
  • Interact with the Sponsor, study sites, and internal associates;
  • Coordinate project meetings
  • Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
  • Create and maintain project timelines;

Qualifications

  • Bachelor's degree in a health sciences field or similar;
  • Prior experience as a Study Coordinator within the pharmaceutical / CRO industry; 
  • Excellent computer skills (word-processing, databases, Excel, Windows)
  • Excellent organizational, and communication skills;
  • Fluency in English and French language.

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