Drug Safety Associate

•     *Complete  all  departmental   project  activities  accurately  in  accordance  with  ICON  SOPs,  Study Specific Procedures, regulatory requirements, and Sponsors processes

•     *Review and process serious adverse events, spontaneously  reported adverse reactions and/or other medically related information per assigned tasks and study specific procedures

•     *Provide  input and review relevant safety tracking  systems for accuracy and quality  and assist with maintaining project files

•     *Perform safety review of clinical and diagnostic data under supervision

•     *Liaise with investigational site, reporter, and/or Sponsor as necessary regarding safety issues under supervision

•     *Attend project team meetings and teleconferences as required

•     Perform other activities as identified and requested by management