Agata Gesiewicz is an experienced professional in pharmacovigilance and risk management with a strong background in compliance and regulatory affairs. Currently serving as EU QPPV and Senior Manager at Lambda Therapeutic Research since February 2019, Agata is responsible for adhering to various European regulations and guidelines. Prior roles include Senior Pharmacovigilance and Risk Management Specialist and Periodic Safety Update Report Specialist at Polpharma, where responsibilities included developing pharmacovigilance agreements, managing safety databases, and preparing risk management documentation. Agata's earlier experience involves positions at Polpharma, science pharma, and University College Dublin, where skills in clinical research, data analysis, and team leadership were honed. Agata holds multiple postgraduate diplomas and a Master's degree in Pharmaceutical Analysis, along with ongoing legal studies.
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