Drug Safety Associate
About the role
This vacancy has now expired. Please see similar roles below...
- As a DSA, you will be expected to perform case validation 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.
- 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.
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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