Adverse Event Report MonitorWe are seeking a dedicated professional to join our close-knit, welcoming team. In this role, you will play a critical part in patient safety by monitoring and processing adverse event reports. If you thrive in a collaborative environment and want to ensure pharmaceutical products meet the highest safety standards, this is the opportunity for you! Responsibilities include monitoring, processing, and distributing adverse event reports and product complaints received from

Also on the board Same function, level within a rung

Level

Mid

Location

St Louis, MO

Occupation

Regulatory Affairs Specialists

Industry

Pharmaceutical Preparation Manufacturing

Posted

8 days ago

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