Drug Safety Associate E/L
About the role
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• *Review and process serious adverse events, spontaneously reported adverse reactions and/or other medically related informationper assigned tasks and study specific procedures
• *Provide input and review relevant safety tracking systems foraccuracy and quality and assist with maintaining project files
• *Perform safety review of clinical and diagnostic data undersupervision
• *Liaise with investigational site, reporter, and/or Sponsor asnecessary regarding safety issues under supervision
• *Attend project team meetings and teleconferences as required
• Perform other activities as identified and requested by management
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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