Drug Safety Specialist - Cambridge

Only for registered members Cambridge, United States

2 weeks ago

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Job summary

Responsible for case processing and/or QC of clinical trial ICSRs and post market case processing from sanctioned countries.

Skills

  • Knowledge of Global and local safety regulations
  • Excellent written and verbal communication skills
  • Experience in ICSR processing in safety database systems such as ArisG, Argus and Veeva

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