ICON Clinical Research Drug Safety Associate in Trivandrum, India

• 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