Drug Safety Associate

• As a DSA, you will be expected to perform case processing for serious adverse events, serious and non-serious adverse drug reactions and other medically-related project information such as adverse events of special interest and clinical endpoints. 
• Provide input and review relevant safety tracking systems for accuracy and quality and assist with maintaining project files.  
• Serve as a resource for investigational sites and ICON personnel on safety-related issues.  
• Assist with generation of study specific procedures and with identifying out of scope activities in conjunction with the MSS Functional Lead.

Role Requirements

• The successful candidate will have relevant clinical research/pharmaceutical industry experience, preferably in pharmacovigilance/drug safety, with knowledge of medical terminology and coding systems. 
• Must be fluent in written and verbal English with good communication skills and basic computer skills.  Detail orientated and capable of working effectively within a team environment. 
• Medical/science background (nursing preferred) and/or bachelor’s degree or local equivalent.

Benefits