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.
Hi, I am Philand I manage this role
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