Case Management Specialist

Zentiva · Prague

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Are you detail-oriented, analytical, and interested in pharmaceuticals and patient safety? Join our Pharmacovigilance team and help ensure that adverse event reports are accurately processed and handled in line with regulatory requirements.


The successful candidate will be responsible for the end-to-end case processing, from case intake and follow-up requests through data entry and quality checks to reporting cases to regulatory authorities or business partners.


Your Responsibilities:



We Require:


Diversity is a fact. Inclusion is an act @Zentiva  
 

At Zentiva, we are a team of 5000 unique talents bonded together by our purpose to provide health and well-being for all generations. We strive daily to create a work culture where everyone feels appreciated, can be their true selves, and contribute to the best of their ability. Seeking for a balanced team across the company, we welcome applications from all qualified candidates with various educational and industry experiences, cultural or ethnical backgrounds, and different life experiences or abilities, regardless of their religious or philosophical beliefs or whomever they choose to love. 

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