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Drug Safety Associate

061403_1571733233

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.

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Two medics at ICON clinical research clinic
The Strategic Role of Site Selection and Activation in Clinical Trials

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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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A Career Focused on Patients: Daniela's Journey at ICON

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10/27/2025

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Daniela’s Journey at ICON Daniela Gutierrez’s career at ICON has been a journey of transition, determination, and purpose. What began as a role in study start-up has evolved into a position deeply

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Daniela shares insights into how collaboration, purpose, and innovation drive every part of her work.

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ICON Careers Spotlight: Chris Maguire, Director of Finance Business Partnering

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Discover how Chris Maguire’s collaborative approach has shaped a rewarding career journey at ICON.

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