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Drug Safety Associate

061403_1571733233

About the role

This vacancy has now expired. Please click here to view live vacancies.

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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Francis' Journey back to ICON

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Publish date

03/26/2026

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Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February

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Lydia's Journey Back to ICON

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Publish date

03/24/2026

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Learn about Lydia's return to ICON and why she felt it was a natural choice.

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03/16/2026

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