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Clinical Research Associate



Company: ToolMedia
City: Laval, Quebec
Industry: Nurse
Date: 19 Apr `06
Employment: Full-Time
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As a CRA you will take part in the monitoring and co-ordination of clinical trials, whilst as SCRA you will provide additional support including site selection, project planning and meeting regulatory requirements.

Requirements
  • Hold a degree in life sciences, or have a nursing/paramedical qualification
  • Have a minimum two years’ experience monitoring clinical trials for a pharmaceutical company/CRO
  • Have strong communication, time management and interpersonal skills
  • Have the ability to work and travel independently
  • Have a flexible approach to work


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