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Senior Drug Safety Associate

Chennai, Tamil Nadu
Permanent
Reference: JR061610_1573794693
Description

* Perform case processing for serious adverse events, serious and non-serious adverse drug reactions, and other medically- related project information, such as adverse events of special interest and clinical endpoints

* Ensure all ICON, Sponsor, and regulatory timeframes are met for the processing and reporting of safety information
* Ensure the completion of all departmental project activities accurately in accordance with ICON standards, regulatory requirements, and contractual obligations to Sponsors

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