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A leading mRNA technology firm in Warsaw is seeking a Specialist in Pharmacovigilance Operations to support global case processing of clinical trial safety reports. The ideal candidate will have a degree in Pharmacy or a related life science, with a minimum of 2 years of experience in drug safety. Key responsibilities include reviewing and documenting adverse events, ensuring compliance with regulations, and contributing to training initiatives. This position offers a chance to impact patient safety through innovative pharmacovigilance tools.
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