Madalina Batista

Expert Quality And Regulatory Affairs at IDT Biologika

Madalina Batista currently serves as an Expert in Quality and Regulatory Affairs at IDT Biologika since August 2022. Prior to this role, Madalina worked as a Regulatory Affairs Manager at CHEPLAPHARM Arzneimittel GmbH from September 2020 to August 2022 and completed a Postgraduate Internship in Clinical Trial Management at Parexel in early 2020. Previous experience includes roles as a Pharmacovigilance Specialist and Project Manager at PrimeVigilance Ltd. from October 2016 to February 2019, a Pharmacy Student Extern at CHU Amiens-Picardie, and trainee positions in community and industrial pharmacies. Madalina holds a Master of Science in Pharmacy from Iuliu Hatieganu University and is currently pursuing postgraduate training through Parexel Academy in clinical monitoring and regulatory affairs. Additionally, Madalina has achieved a B2 level in German through Volkshochschule Esslingen.

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Berlin, Germany

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IDT Biologika

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Spezialisiert auf Auftragsentwicklung und Auftragsfertigung von Virusimpfstoffen, viralen Vektoren und Biologika


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1,001-5,000

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