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    CRA (Clinical Research Associate)  
To assure the implementation of project plans as assigned, Ethics committee and competent authority regulatory submissions of clinical trials applications, site monitoring & site management responsibility according to ICH Guidelines and GCP, local regulations, study requirements and SOPs.

  • Certified CRA
  • University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution
  • In lieu of the above requirement, candidates with with experience as CTA or Study Coordinator will be considered
  • Fluent in local office language and in English, both written and verbal
  • Excellent interpersonal relationships and team player
  • Energetic, Effective, Assertive and well motivated
  • Excellent planning and organization skills
  • Work under pressure and independently
  • Service oriented
  • Prioritizing workload
  • Excellent computer skills including: Outlook, Word, Excel, PowerPoint
  • Vehicle

Work is Sunday-Thursday 8:00-17:00.
Location in the area of Modiin.
Send your CV via email only:
Only relevant applications will be answered.