Drug Safety Associate
About the role
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Drug Safety Associate role within ICON:
The Drug Safety Associate prepares and performs quality checks of regulatory documentation packets and coordinates the timely completion and submission of required reports to Health Authorities, Ethic Committees, Principal Investigators and third parties. You will also ensure compliance with regulatory reporting requirements for safety reporting (pre-marketing, post-marketing, device and drug) and/or other medically related information per assigned tasks and project specific procedures.
To succeed you will need:
We are seeking candidates with a medical/science background (nursing preferred) and/or bachelor's degree or local equivalent. Minimum of 1-2 years related experience in Pharmacovigilance/Clinical Research. To be successful you will be expected to be proficient in Microsoft Office skills (Word, Excel, and Access). Have good communication skills, be fluent in written and verbal English, detail-oriented and have the ability to work effectively within a team environment.
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. Learn more about Our Culture at ICON
Day in the life
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Our PeopleContent type
BlogsPublish date
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
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Our PeopleContent type
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11/13/2025
Summary
A Career Built on Patient Impact: Victoria DeVeaugh Geiss's Journey at ICON Victoria DeVeaugh Geiss has spent more than two decades in clinical research, and one thing has stayed constant throughout
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IndustryContent type
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Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
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