Drug Safety Associate
About the role
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- Your primary responsibility will be validating and quality checking safety database fields on assigned projects.
- You will also provide input for and review relevant safety tracking systems for accuracy/quality and perform safety review of clinical data (case report forms) and patient labs.
- You will also be responsible for documenting and processing serious adverse event cases within ICON, regulatory authorities and sponsor regulations and timeframes.
- With a science degree, pharmacy or nursing background or equivalent, you will have previous experience in a drug safety environment together with strong knowledge of medical terminology.
- You will have knowledge of drug safety databases, preferably ARGUS.
- You will have the ability to produce high quality work, with meticulous attention to detail.
- You will be fluent in verbal and written English, with excellent communication skills.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Read more
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